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MEDI MANUFACTURING, INC. · Model KAK2M5W5 · UDI-DI 00636257014752

IPM
6
510(k) clearances
6
Adverse events
1
Recalls
148
Facilities

Description

!30-40 SHRINKER AK 10" MED BLACK SZ 5

Recalls

DateFirmReason
2021-04-20WillowWood Global Llcthe firm discovered that, starting on April 1, 2020, a 3/8 dowel pin was used in place of the 5/8 pin. Over time, the shorter pin may not engage in either the upper or lower body,

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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.