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FDA Drug information

Leukotrap WB System

Read time: 1 mins
Marketing start date: 23 Dec 2024

Summary of product characteristics


Adverse Reactions

ADVERSE REACTIONS There are no known potential adverse reactions associated specifically with the Leukotrap WB System with CPDA-1.

Description

DESCRIPTION CPDA-1 Blood Collection Set, Double Bag with WBF2 Filter and Sampling System Instruction for Use for Systems Containing a Y Sampling Site (YSS) or Sample Diversion Pouch (with or without a pre-attached Samp Lok Vacuum Tube Holder). Refer to unit foil package label for specific product description being used. Sterile, nonpyrogenic fluid path. Sterilized by steam. Rx only. This product is free of natural rubber latex.

Indications And Usage

INDICATIONS AND USAGE Indicated for collection of blood and preparation of red blood cells and plasma with pre-storage leukocyte reduction. Platelet concentrates are not intended to be made with this product.

Warnings

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

Effective Time

20230719

Version

4

Spl Product Data Elements

Leukotrap WB System CPDA-1 Blood Bag Collection System DEXTROSE MONOHYDRATE ANHYDROUS DEXTROSE SODIUM CITRATE ANHYDROUS CITRIC ACID SODIUM CATION CITRIC ACID MONOHYDRATE ANHYDROUS CITRIC ACID ADENINE ADENINE SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE PHOSPHATE ION SODIUM CATION

Application Number

BN800077

Brand Name

Leukotrap WB System

Generic Name

CPDA-1 Blood Bag Collection System

Product Ndc

53157-736

Product Type

HUMAN PRESCRIPTION DRUG

Route

INTRAVENOUS

Package Label Principal Display Panel

PACKAGE/LABEL PRINCIPAL DISPLAY PANEL Envelope Label Collection Bag Label Plasma Bag Label Transfer Bag Label Envelope Label Collection Bag Label Plasma Bag Label Transfer Bag Label

Spl Unclassified Section

I. BLOOD COLLECTION INSTRUCTIONS FOR SYSTEMS CONTAINING A Y SAMPLING SITE (YSS) ONLY 1. Load blood agitation device or suspend blood bag on donor scale and adjust donor scale to desired collection gross weight as per manufacturer's instructions. 2. Clamp donor tubing between the Donor Care ® Needle Guard (DCNG) and Y Sampling Site. 3. Secure donor tubing above the Y connector and disinfect site of phlebotomy. 4. If using blood pressure cuff, inflate to not more than 60 mm Hg. 5. Remove donor needle cover and accomplish phlebotomy. 6. Release clamp and ensure there is blood flow. Reduce pressure as required. 7. Slide the DCNG midway over the needle hub and securely tape DCNG to the donor's arm as close to the top of the DCNG as possible. Note: If blood flow is slow, slide DCNG away from the needle hub, adjust and re-engage DCNG. If repeated needle adjustment is necessary, slide DCNG away from the needle hub and re-engage at the end of blood collection. 8. Collect appropriate volume of blood into collection bag, as indicated on packaging. Note: Mix blood and anticoagulant frequently during collection, for example, once every 45 seconds, and immediately after collection. If blood agitation device is used, follow manufacturer's operating instructions. 9. After required amount of blood has been collected, seal donor tubing between Y Sampling Site and the collection bag.* 10. For blood sampling, remove the Y Sampling Site needle cover. Ensure the protective sheath is in place over the sampling needle. 11. Fasten the vacuum tube holder on to the base of the sampling needle. 12. Collect blood samples into vacuum tubes. 13. Ensure the vacuum tubes are centered within the vacuum tube holder during sample collection. 14. Maintain forward pressure on the vacuum tubes during sample collection. Note: After the last tube is collected, it is recommended that the vacuum tube holder be left in place. 15. After blood samples are collected, clamp donor tubing between the Y Sampling Site and DCNG, as close as possible to the DCNG. 16. Release any remaining pressure from the donor's arm. 17. DCNG must be held stationary while the needle is withdrawn into it. While holding sides of DCNG near the front, grasp the tubing below the clamp and pull the needle into the DCNG until it locks into place, and the needle hub engages the bottom of the DCNG. 18. Insert the DCNG into the vacuum tube holder. Note: It is recommended that the DCNG be inserted securely into the vacuum tube holder prior to discarding. 19. Seal donor tubing adjacent to DCNG.* Detach and discard needle, DCNG, Y Sampling Site and tubing.* 20. Strip tubing between seal and collection bag. 21. Continue to “Processing Instructions”, Section IV, Step 1.

References

REFERENCES HAEMONETICS and THE Blood Management Company are trademarks of Haemonetics Corporation. DonorCare and SampLok are registered trademarks of ITL Corporation, Canberra, Australia. Manufactured for: Haemonetics Corporation 400 Wood Road Braintree, MA 02184, USA By: Haemonetics Manufacturing Inc. 1630 Industrial Park Street Covina, CA 91722, USA www.haemonetics.com 800-537-2802

How Supplied

HOW SUPPLIED Each shipping case contains 6 foil envelopes. Within each foil envelope resides 3 units of the collection system. Each unit consists of a collection bag with 70 ml of CPDA-1 solution and two empty bags.

Precautions

GENERALPRECAUTIONS Use Aseptic Technique. Use only if solution is clear. Store CPDA-1 preserved red blood cells at 1—6 °C for up to 35 days and use as indicated. * During processing, always observe the following precautions: 1. Sealing should be done in a manner that avoids fluid splatter. 2. Always dispose of blood-contaminated products in a manner consistent with established BIOHAZARD safety procedures.

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Disclaimer

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