Class III — Biomedical Polymers, Inc.
| Recalling firm | BIOMEDICAL POLYMERS, INC. dba BMP Medical |
|---|---|
| Registered facility | Biomedical Polymers, Inc. (the firm's only registered facility) |
| Classification | Class III |
| Status | Terminated |
| 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. |
| Product | Hemo-Drop Blood Dispenser, Part Number BMP-HEMODROP, used for preparing blood samples. |
| Quantity | 108,000 |
| Distribution | US nationwide distribution. |
| Initiated | 2019-09-18 |
| Classified | 2019-11-05 |
| Terminated | 2020-09-15 |
| Recall number | Z-0286-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class III recall — Biomedical Polymers, Inc. (Z-0286-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83965/
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