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Pinpoint GT
Bard Access Systems, Inc. · Model 9770647 · UDI-DI 00801741128929
PVZ
Prescription
1
510(k) clearances
0
Adverse events
1
Recalls
3
Facilities
Description
Hypodermic Pinpoint GT Needle
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-07-10 | Stryker Corporation | Potential for current software to miscount when scanning in multiple sponge-products from the same unique sponge-pack type |
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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.