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Arthrex®

ARTHREX, INC. · Model AR-7199 · UDI-DI 00888867041257

LZB Prescription
5
510(k) clearances
1
Adverse events
1
Recalls
73
Facilities

Description

FINGERSHIELDS

Recalls

DateFirmReason
2016-03-31American Surgical CompanyProduct packaging defective compromising sterility

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.