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Hu-Friedy Mfg. Co., LLC
HU-FRIEDY MFG. CO., LLC · Model PSN8660P · UDI-DI 10889950001896
GAW
Prescription
10
510(k) clearances
20,303
Adverse events (226 deaths)
33
Recalls
112
Facilities
Description
6-0 BLUE POLYPROPYLENE SUTURE 18", C-22 NEEDLE 16.2MM, 3/8 CIRCLE REVERSE CUT
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-09-17 | Henry Schein Inc. | Products lack 510(k) clearance. |
| 2026-09-17 | Henry Schein Inc. | Products lack 510(k) clearance. |
| 2026-09-17 | Henry Schein Inc. | Products lack 510(k) clearance. |
| 2026-09-17 | Henry Schein Inc. | Products lack 510(k) clearance. |
| 2026-09-17 | Henry Schein Inc. | Products lack 510(k) clearance. |
| 2026-06-24 | Covidien, LP | Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of v |
| 2026-06-24 | Covidien, LP | Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of v |
| 2024-12-20 | Ethicon, LLC | Sutures may have an open seal on the primary packaging, due to a manufacturing issue on a specific machine, and if issue is undetected could lead to breach in sterility, could intr |
| 2024-12-20 | Ethicon, LLC | Sutures may have an open seal on the primary packaging, due to a manufacturing issue on a specific machine, and if issue is undetected could lead to breach in sterility, could intr |
| 2024-12-20 | Ethicon, LLC | Sutures may have an open seal on the primary packaging, due to a manufacturing issue on a specific machine, and if issue is undetected could lead to breach in sterility, could intr |
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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.