Reported Nov 13, 2019 · Terminated

Manual Diff Dropper, Part Number CHB4001, used for preparing blood samples.

Biomedical Polymers, Inc.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Biomedical Polymers, Inc. · 16 Chocksett Rd · Sterling, MA · 01564-2336

Is this the product you have?

  • Manual Diff Dropper, Part Number CHB4001, used for preparing blood samples.
Lot codes and dates
  • UPC(01) 50885380116009
  • Lot numbers
    • 20180709A1C
    • 20180717A1C
Amount recalled
2,052,000

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

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.

This product is unlikely to cause harm, but it breaks a safety or labelling rule.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Sep 15, 2020 · Data as of Sep 19, 5:32 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.