Heparin Sodium
Recalling Firm: Hospira Inc.
Recall Initiation Date: Thursday September 11th, 2014
Reason for Recall: Presence of Particulate Matter: A particulate, confirmed as human hair, was found sealed between the tube and film at the round seal of the unused administrative port of the container.
Cefepime Hydrochloride And Dextrose
Recalling Firm: B. Braun Medical Inc
Recall Initiation Date: Thursday November 21st, 2013
Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
Venlafaxine Hydrochloride
Recalling Firm: Greenstone Llc
Recall Initiation Date: Thursday March 6th, 2014
Reason for Recall: Presence of Foreign Tablets/Capsules: A Pharmacist reported a foreign capsule with markings (TKN 250) and identified as a Tikosyn (dofetilide) capsule in a lot of Effexor XR 150 mg capsules that was packaged in the same packaging campaign as this Venlafaxine HCl lot.
Venlafaxine Hydrochloride
Recalling Firm: Greenstone Llc
Recall Initiation Date: Thursday March 6th, 2014
Reason for Recall: Presence of Foreign Tablets/Capsules: A Pharmacist reported a foreign capsule with markings (TKN 250) and identified as a Tikosyn (dofetilide) capsule in a lot of Effexor XR 150 mg capsules that was packaged in the same packaging campaign as this Venlafaxine HCl lot.
Procalamine
Recalling Firm: B. Braun Medical Inc
Recall Initiation Date: Thursday November 21st, 2013
Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
Sodium Chloride
Recalling Firm: B. Braun Medical Inc
Recall Initiation Date: Thursday November 21st, 2013
Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
Aminosyn Ii
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday August 30th, 2013
Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint of particulate matter, identified as a human hair, visible in the injection port and primary container.
Freamine Hbc
Recalling Firm: B. Braun Medical Inc
Recall Initiation Date: Thursday November 21st, 2013
Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
Metformin Hydrochloride
Recalling Firm: Shamrock Medical Solutions Group LLC
Recall Initiation Date: Tuesday September 27th, 2011
Reason for Recall: Labeling: Label Mix up; product labeled did not indicated Extended Release
Pain Relief
Recalling Firm: Shamrock Medical Solutions Group LLC
Recall Initiation Date: Tuesday September 27th, 2011
Reason for Recall: Labeling: Label Mix up; product labeled did not indicated Extended Release
Ibandronate Sodium
Recalling Firm: Shamrock Medical Solutions Group LLC
Recall Initiation Date: Tuesday September 27th, 2011
Reason for Recall: Labeling: Label Mix up; product labeled did not indicated Extended Release
Clinimix E
Recalling Firm: Baxter Healthcare Corp.
Recall Initiation Date: Monday November 18th, 2013
Reason for Recall: Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.
Coumadin
Recalling Firm: Bristol-Meyers Squibb
Recall Initiation Date: Monday May 12th, 2014
Reason for Recall: Presence of Particulate Matter: particulate matter identified as metallic-like and non-metallic cellulose fiber particles found in retain vials
Atorvastatin Calcium
Recalling Firm: Shire Human Genetic Therapies, Inc.
Recall Initiation Date: Friday March 14th, 2014
Reason for Recall: Presence of Particulate Matter; Particulates identified as stainless steel and barium sulfate.
Nitroglycerin In Dextrose
Recalling Firm: Baxter Healthcare Corp.
Recall Initiation Date: Monday November 18th, 2013
Reason for Recall: Presence of Particulate Matter; particulate matter in one vial identified as silicone rubber and EPDM rubber from the vial stopper.
Effexor Xr
Recalling Firm: Pfizer Us Pharmaceutical Group
Recall Initiation Date: Thursday March 6th, 2014
Reason for Recall: Presence of Foreign Tablets/Capsules: A Pharmacist reported that a bottle of Effexor XR 150 mg capsules contained a single peach colored capsule printed TKN250 which was identified as a Tikosyn (dofetilide) capsule.
Effexor Xr
Recalling Firm: Pfizer Us Pharmaceutical Group
Recall Initiation Date: Thursday March 6th, 2014
Reason for Recall: Presence of Foreign Tablets/Capsules: A Pharmacist reported that a bottle of Effexor XR 150 mg capsules contained a single peach colored capsule printed TKN250 which was identified as a Tikosyn (dofetilide) capsule.
Amino Acids
Recalling Firm: B. Braun Medical Inc
Recall Initiation Date: Thursday November 21st, 2013
Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
Clinimix
Recalling Firm: Baxter Healthcare Corp.
Recall Initiation Date: Monday November 18th, 2013
Reason for Recall: Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.
Dobutamine Hydrochloride
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday January 10th, 2014
Reason for Recall: Presence of Particulate Matter: Discolored solution due to a chip in the glass at the neck of the vial, also glass particulate was found within the solution.
Trophamine
Recalling Firm: B. Braun Medical Inc
Recall Initiation Date: Thursday November 21st, 2013
Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
Potassium Chloride
Recalling Firm: Baxter Healthcare Corp.
Recall Initiation Date: Friday July 11th, 2014
Reason for Recall: Presence of Particulate Matter: particulate matter identified as fibers and/or plastics.
Cefoxitin And Dextrose
Recalling Firm: B. Braun Medical Inc
Recall Initiation Date: Thursday November 21st, 2013
Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
Acetylcysteine Solution
Recalling Firm: Ben Venue Laboratories Inc
Recall Initiation Date: Friday February 14th, 2014
Reason for Recall: Presence of Particulate Matter: During a review of retain samples, the firm found a glass particulate in one lot of Acetylcysteine Solution
Acetylcysteine Solution
Recalling Firm: Ben Venue Laboratories Inc
Recall Initiation Date: Friday February 14th, 2014
Reason for Recall: Presence of Particulate Matter: During a review of retain samples, the firm found a glass particulate in one lot of Acetylcysteine Solution
Mlk F4 Kit
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday October 18th, 2013
Reason for Recall: Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.
Marbeta 25 Kit
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday October 18th, 2013
Reason for Recall: Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.
Marcaine
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday October 18th, 2013
Reason for Recall: Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.
Marcaine
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday October 18th, 2013
Reason for Recall: Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.
Marcaine
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday October 18th, 2013
Reason for Recall: Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.
Marcaine
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday October 18th, 2013
Reason for Recall: Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.
Marcaine
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday October 18th, 2013
Reason for Recall: Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.
Marcaine
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday October 18th, 2013
Reason for Recall: Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.
Soliris
Recalling Firm: Alexion Pharmaceuticals, Inc.
Recall Initiation Date: Monday November 4th, 2013
Reason for Recall: Presence of Particulate Matter: Failed the appearance test for the presence of visible particles.
Hyperlyte Cr
Recalling Firm: B. Braun Medical Inc
Recall Initiation Date: Thursday November 21st, 2013
Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
Cefazolin Sodium Solution
Recalling Firm: B. Braun Medical Inc
Recall Initiation Date: Thursday November 21st, 2013
Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
Sodium Chloride
Recalling Firm: Hospira Inc.
Recall Initiation Date: Tuesday January 20th, 2015
Reason for Recall: Presence of Particulate Matter; Hospira has identified the particulate as a human hair, sealed in the bag at the additive port area.
Propofol
Recalling Firm: Hospira Inc.
Recall Initiation Date: Monday October 6th, 2014
Reason for Recall: Temperature Abuse: Products experienced uncontrolled temperature excursions during transit.
Propofol
Recalling Firm: Hospira Inc.
Recall Initiation Date: Monday October 6th, 2014
Reason for Recall: Temperature Abuse: Products experienced uncontrolled temperature excursions during transit.
Lactated Ringers
Recalling Firm: Baxter Healthcare Corp.
Recall Initiation Date: Tuesday March 24th, 2015
Reason for Recall: Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Lactated Ringers
Recalling Firm: Baxter Healthcare Corp.
Recall Initiation Date: Tuesday March 24th, 2015
Reason for Recall: Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Mucinex Fast-max Cold And Sinus
Recalling Firm: Reckitt Benckiser LLC
Recall Initiation Date: Wednesday April 15th, 2015
Reason for Recall: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing certain Active Ingredients such as acetaminophen, phenylephrine, dextromethorphan, diphenhydramine, and/or guaifenesin. As a result certain safety warnings associated with those ingredients may also be missing.
Mucinex Fast-max Day Time Severe Cold And Mucinex Fast-max Night Time Cold And Flu Maximum Strength
Recalling Firm: Reckitt Benckiser LLC
Recall Initiation Date: Wednesday April 15th, 2015
Reason for Recall: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing certain Active Ingredients such as acetaminophen, phenylephrine, dextromethorphan, diphenhydramine, and/or guaifenesin. As a result certain safety warnings associated with those ingredients may also be missing.
Lactated Ringers
Recalling Firm: Hospira Inc.
Recall Initiation Date: Wednesday March 11th, 2015
Reason for Recall: Non-Sterility: Confirmed customer report of dark, fibrous particulates floating within the solution of the primary container, which were subsequently identified as mold
Bupivacaine Hydrochloride And Epinephrine
Recalling Firm: Hospira Inc.
Recall Initiation Date: Thursday April 23rd, 2015
Reason for Recall: Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.
15922-20 Continuous Epidural 18g Tuohy
Recalling Firm: Hospira Inc.
Recall Initiation Date: Thursday April 23rd, 2015
Reason for Recall: Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.
A3852-1727 Combined Spinalepidural 17g Tuohy
Recalling Firm: Hospira Inc.
Recall Initiation Date: Thursday April 23rd, 2015
Reason for Recall: Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.
Bupivacaine Hydrochloride
Recalling Firm: Hospira Inc.
Recall Initiation Date: Thursday April 23rd, 2015
Reason for Recall: Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.
Atenolol
Recalling Firm: Hospira Inc.
Recall Initiation Date: Thursday April 23rd, 2015
Reason for Recall: Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.
Bupivacaine Hydrochloride
Recalling Firm: Hospira Inc.
Recall Initiation Date: Thursday April 23rd, 2015
Reason for Recall: Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.
Bupivacaine Hydrochloride
Recalling Firm: Hospira Inc.
Recall Initiation Date: Thursday April 23rd, 2015
Reason for Recall: Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.
Mucinex Fast-max Day Time Severe Congestion And Cough And Mucinex Fast-max Night Time Cold And Flu Maximum Strength
Recalling Firm: Reckitt Benckiser LLC
Recall Initiation Date: Wednesday April 15th, 2015
Reason for Recall: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing certain Active Ingredients such as acetaminophen, phenylephrine, dextromethorphan, diphenhydramine, and/or guaifenesin. As a result certain safety warnings associated with those ingredients may also be missing.
Magnesium Sulfate In Dextrose
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday March 6th, 2015
Reason for Recall: Labeling: Wrong Bar Code: There is a potential for some units to be mislabeled with an incorrect barcode on the immediate container that scans as heparin sodium 2000 USP units/1000 mL in 0.9% in sodium chloride injection.
Carboplatin
Recalling Firm: Mylan Institutional LLC
Recall Initiation Date: Wednesday March 18th, 2015
Reason for Recall: Presence of Particulate Matter: visible foreign particulate matter observed during testing of retention samples.
Lidocaine Hydrochloride
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday April 18th, 2014
Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.
Mucus Relief
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday April 18th, 2014
Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.
A3207-22 Portex Amniocentesis 22g Quincke
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday April 18th, 2014
Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.
Mlk F4 Kit
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday April 18th, 2014
Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.
Marlido 25 Kit
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday April 18th, 2014
Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.
Lidocaine Hydrochloride
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday April 18th, 2014
Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.
Lidocaine Hydrochloride
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday April 18th, 2014
Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.
Lidocaine Hydrochloride
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday April 18th, 2014
Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.
Lidocaine Hydrochloride
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday April 18th, 2014
Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.
Lidocaine Hydrochloride
Recalling Firm: Hospira Inc.
Recall Initiation Date: Friday April 18th, 2014
Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.
Gemcitabine Hydrochloride
Recalling Firm: Mylan Institutional LLC
Recall Initiation Date: Monday March 23rd, 2015
Reason for Recall: Presence of Particulate Matter: visible foreign particulate matter observed during testing of retention samples.
Amiodarone Hydrochloride
Recalling Firm: Baxter Healthcare Corp.
Recall Initiation Date: Friday July 17th, 2015
Reason for Recall: Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.
Sodium Chloride
Recalling Firm: Baxter Healthcare Corp.
Recall Initiation Date: Friday July 17th, 2015
Reason for Recall: Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.
Adrucil
Recalling Firm: Teva Pharmaceuticals USA
Recall Initiation Date: Friday July 24th, 2015
Reason for Recall: Presence of Particulate Matter: silcone rubber and fluorouracil crystals found floating in solution
Sodium Chloride
Recalling Firm: Hospira Inc.
Recall Initiation Date: Thursday March 5th, 2015
Reason for Recall: Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution.
Mucinex Fast-max Day Time Severe Cold And Mucinex Fast-max Night Time Cold And Flu Maximum Strength
Recalling Firm: Reckitt Benckiser LLC
Recall Initiation Date: Wednesday April 15th, 2015
Reason for Recall: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing certain Active Ingredients such as acetaminophen, phenylephrine, dextromethorphan, diphenhydramine, and/or guaifenesin. As a result certain safety warnings associated with those ingredients may also be missing.
Mucinex Fast-max Cold
Recalling Firm: Reckitt Benckiser LLC
Recall Initiation Date: Wednesday April 15th, 2015
Reason for Recall: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing certain Active Ingredients such as acetaminophen, phenylephrine, dextromethorphan, diphenhydramine, and/or guaifenesin. As a result certain safety warnings associated with those ingredients may also be missing.
Dextrose
Recalling Firm: Baxter Healthcare Corp.
Recall Initiation Date: Tuesday March 24th, 2015
Reason for Recall: Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Protonix Delayed-release
Recalling Firm: Baxter Healthcare Corp.
Recall Initiation Date: Tuesday March 24th, 2015
Reason for Recall: Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Sodium Chloride
Recalling Firm: Baxter Healthcare Corp.
Recall Initiation Date: Friday July 17th, 2015
Reason for Recall: Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.
Gemcitabine Hydrochloride
Recalling Firm: Mylan Institutional LLC
Recall Initiation Date: Monday March 23rd, 2015
Reason for Recall: Presence of Particulate Matter: visible foreign particulate matter observed during testing of retention samples.
Lactated Ringers And Dextrose
Recalling Firm: Hospira Inc.
Recall Initiation Date: Thursday July 10th, 2014
Reason for Recall: Non-Sterility: Confirmed customer complaint of particulate matter floating within the solution of the primary container, consistent with mold.