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G7 PROVISIONAL SHELL

Biomet Orthopedics, LLC · Model 010002467 · UDI-DI 00880304564640

PBIOQIOQHLZOJDILPHOQGKWZLWZ Prescription
1
510(k) clearances
2,276
Adverse events (2 deaths)
2
Recalls
31
Facilities

Recalls

DateFirmReason
2014-05-07Biomet, Inc.Guide rod may fracture during impaction of the acetabular shell and be retained in the inserter or the patient and could result in a delay in surgery.
2014-05-07Biomet, Inc.Guide rod may fracture during impaction of the acetabular shell and be retained in the inserter or the patient and could result in a delay in surgery.

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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.