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Henry Schein

HENRY SCHEIN, INC. · Model 1000555 · UDI-DI 00304040043912

EMO
0
510(k) clearances
0
Adverse events
1
Recalls
62
Facilities

Description

Knife Kirkland DE 15K/16K

Recalls

DateFirmReason
2018-03-28Ace Surgical Supply Co., Inc.The product inside the package is incorrect. A single blade shoe was mistakenly packaged instead of a double blade.

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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.