Home › HU-FRIEDY MFG. CO., LLC › Hu-Friedy Mfg. Co., LLC
Hu-Friedy Mfg. Co., LLC
HU-FRIEDY MFG. CO., LLC · Model PSNR7772L · UDI-DI 10889950002084
GAO
Prescription
4
510(k) clearances
601
Adverse events (10 deaths)
1
Recalls
18
Facilities
Description
3-0 GREEN POLYESTER SUTURE 18", C-6 NEEDLE 18.7MM, 3/8 CIRCLE REVERSE CUT
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-02-11 | EXP Pharmaceutical Services Corp | EXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality system and instead relied on the fact that its vendors were re |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.
