Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0634-2022 — Universal Chuck-The Universal Chuck is an Instrument Handle provided as an alternative instrument available for use in the TN-ADVANCED" Tibial Nailing System (TNA), TFN-ADVANCED" Proximal Femoral Nailing System (TFNA), RFN-ADVANCED" Retrograde Femoral Nailing System (RFNA), FRN-ADVANCED" Femoral Rec

U.S. FDA — Device Enforcement · United States · 2021-12-22 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0634-2022
Date of alert
2021-12-22
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Synthes (USA) Products LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
20013101
Reported risk: Top cap may loosen and detach if the Universal Chuck becomes jammed and the user attempts to manually free the device, internal ball bearings may fall out onto the surgical field and cause surgical delay or, and if not recovered, adverse tissue reaction and infection.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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