Bioseal Inc.
BIOSEAL · Model 17396/50 · UDI-DI 00630094739656
1
510(k) clearances
29
Adverse events
1
Recalls
35
Facilities
Description
Vacutainer Glass Tube
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-12-19 | OriGen Biomedical, Inc. | Accessory sets contain a syringes not yet qualified for the accessory's intended purpose; due to design changes to the syringe barrels and a polypropylene resin change that resulte |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.