⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Zimmer, Inc.: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815509300 Software

Medical DevicesSource: FDA (device) · Date: 2025-12-31

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The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.

Company / brand
Zimmer, Inc.
Product
Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815509300 Software Version: N/A Product Description: Affixus 9 mm, Length 300 mm, Right, Trochanteric Nail Component: N/A
Reason / hazard
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
Classification
Class II
Status
Ongoing
Distribution / sold at
US Nationwide distribution in the states of AL, AZ, CA, FL, IN, KY, MA, MO, MT, NC, NM, RI, TX, UT.
Recall initiated
2025-12-02
Code info
Lot Code: Model No 815509300 ; UDI-DI (01)00887868143519(17)340823(10)66717550 ; Lot Number 66717550
Product quantity
11
Voluntary mandated
Voluntary: Firm initiated
City
Warsaw
State
IN
Country
United States
Event id
98069
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