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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Device

Biomedical Polymers, Inc.: The metal cannula of the device either broke and the broken piece left in the blood specimen tube, or slid back into the plastic portion of the device instead of piercing the tube.

Agency Publication Date: November 5, 2019
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Affected Products

Product: Hemo-Drop Blood Dispenser, Part Number BMP-HEMODROP, used for preparing blood samples.

UPC: (01) 20885380116008 Lot: 20180717A1

Lot Numbers:
20180717A1
Product: Manual Diff Dropper, Part Number CHB4001, used for preparing blood samples.

UPC: (01) 50885380116009 Lot numbers: 20180709A1C, 20180717A1C

Lot Numbers:
numbers

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 83965
Status: Resolved
Manufacturer: Biomedical Polymers, Inc.
Manufactured In: United States
Units Affected: 2 products (108,000; 2,052,000)

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.