This site is intended for healthcare professionals
Abstract digital waveforms in blue and purple
FDA Drug information

CPDA-1 Blood Collection System

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

Summary of product characteristics


Adverse Reactions

ADVERSE REACTIONS There are no known potential adverse reactions associated specifically with the CPDA-1 Blood Collection Set with Sampling System.

Description

DESCRIPTION CPDA-1 Blood Collection Set with 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 For collection of blood and preparation of red blood cells, plasma and platelets. Platelets are not intended to be produced when using ‘doubles’ .

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

20200102

Version

3

Spl Product Data Elements

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

Application Number

BN800077

Brand Name

CPDA-1 Blood Collection System

Generic Name

Blood Collection System

Product Ndc

53157-130

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 Envelope Label Collection Bag Label Plasma 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 IFU P/N 147130924

How Supplied

HOW SUPPLIED Each shipping case contains 8 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 one empty bag.

Precautions

GENERALPRECAUTIONS Use Aseptic Technique. Use only if solution is clear. If preparing a platelet concentrate, the platelet-rich plasma should be separated from the red blood cells within 8 hours after blood collection. If preparing fresh frozen plasma, separate from the red blood cells and place in the freezer at -18 °C or colder within 8 hours after collection. 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.

Learning Zones

The Learning Zones are an educational resource for healthcare professionals that provide medical information on the epidemiology, pathophysiology and burden of disease, as well as diagnostic techniques and treatment regimens.

Disclaimer

The drug Prescribing Information (PI), including indications, contra-indications, interactions, etc, has been developed using the U.S. Food & Drug Administration (FDA) as a source (www.fda.gov).

Medthority offers the whole library of PI documents from the FDA. Medthority will not be held liable for explicit or implicit errors, or missing data.

Drugs appearing in this section are approved by the FDA. For regions outside of the United States, this content is for informational purposes only and may not be aligned with local regulatory approvals or guidance.