Leukotrap – Cp2d Solution

Leukotrap – Cp2d Solution

Leukotrap – Cp2d Solution Recall

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Questions & Answers

Side Effects & Adverse Reactions

Failure to achieve and maintain a closed system during processing would result in a product that must be transfused within 24 hours.

Legal Issues

There is currently no legal information available for this drug.

FDA Safety Alerts

There are currently no FDA safety alerts available for this drug.

Manufacturer Warnings

There is currently no manufacturer warning information available for this drug.

FDA Labeling Changes

There are currently no FDA labeling changes available for this drug.

Uses

Whole blood; for use in blood collection.

History

There is currently no drug history available for this drug.

Other Information

For collection of blood and preparation of red blood cells, plasma and platelets with pre-storage leukocyte reduction.

Instruction for Use for Systems Containing a Y Sampling Site (YSS) or Sample Diversion Pouch (with or without a pre-attached SampLok™ Vacuum Tube Holder).

Refer to unit foil package label for specific product description being used.

Sterile, non-pyrogenic fluid path. Sterilized by steam.

Rx only.

Illustration

Collection system with sample diversion pouch

FigA

123-93 Collection System with Sample Diversion Pouch

Leukotrap – Cp2d Solution Manufacturers


  • Haemonetics Manufacturing Inc
    Leukotrap – Cp2d Solution (Anticoagulant Citrate Phosphate Double Dextrose ) Solution Leukotrap – As-3 Solution (Additive Solution – 3) Solution [Haemonetics Manufacturing Inc]

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