Biomedical Polymers, Inc. recalls Manual Diff Dropper, Part Number CHB4001, used for preparing blood samples.
- Recall date
- September 18, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0287-2020
- FDA classification
- Class III
- Brand / firm
- Biomedical Polymers, Inc.
- Sold / distributed
- US nationwide distribution.
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.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Manual Diff Dropper, Part Number CHB4001, used for preparing blood samples.
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