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ITST®

Zimmer, Inc. · Model 2256-180-14 · UDI-DI 00889024046979

NDEHSB Prescription
2
510(k) clearances
4
Adverse events
1
Recalls
0
Facilities

Recalls

DateFirmReason
2016-11-09Stryker Howmedica Osteonics Corp.A review of packaging revealed the seal integrity of the pouch may be compromised. More specifically, there is a potential that the sterile pouch is not sealed at one end due to a

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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.