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Trimed, INC. · Model MPP-WIRE · UDI-DI 00842188109072

NDL Prescription
1
510(k) clearances
55
Adverse events
1
Recalls
11
Facilities

Description

Bent K-Wire 1.6mm

Recalls

DateFirmReason
2019-10-02Exactech, Inc.Potential for the 2.4mm x 2.5 Fluted Pin Pouch to contain a single pin rather than four (4) as intended.

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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.