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PROSTAGRIP™
LSI Solutions, Inc. · Model 081358 · UDI-DI 00850012846338
FBX
Prescription
1
510(k) clearances
16
Adverse events
1
Recalls
54
Facilities
Description
PROSTAGRIP™ DEVICE
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
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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.