FDA Device recall Z-0287-2020
Manual Diff Dropper, Part Number CHB4001, used for preparing blood samples
- FDA Device
- Class III
- terminated
- Published 2019-11-13
On 2019-11-13 the FDA classified a Class III recall of Manual Diff Dropper, Part Number CHB4001, used for preparing blood samples by Biomedical Polymers, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0287-2020 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2019-09-18 |
| Published | 2019-11-13 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Biomedical Polymers |
| Distribution | US |
Product
Manual Diff Dropper, Part Number CHB4001, used for preparing blood samples.
Reason
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.
Identifiers
| code_info | UPC: (01) 50885380116009 Lot numbers: 20180709A1C, 20180717A1C |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0287-2020%22
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