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Zimmer GmbH recalls Biolox Option Taper Sleeve, Type 1 Taper, Standard Neck - Indicated for use in total hip replacement with cemented or no

Recalled September 18, 2024 · FDA recall Z-3132-2024 · Zimmer

Hazard
Mislabeled: Incorrect sleeve in the packaging. The outer packaging is labeled as a standard neck sleeve, however, the product within the box is a -6mm neck sleeve, and vice versa. The neck of the sleeve can be identified by the device etching as either STD or -6 · FDA Class II
Units
69 units
Sold at
Worldwide distribution - US Nationwide and the countries of Japan, Netherlands.

Description

Mislabeled: Incorrect sleeve in the packaging. The outer packaging is labeled as a standard neck sleeve, however, the product within the box is a -6mm neck sleeve, and vice versa. The neck of the sleeve can be identified by the device etching as either STD or -6

Product
Biolox Option Taper Sleeve, Type 1 Taper, Standard Neck - Indicated for use in total hip replacement with cemented or non-cemented femoral and acetabular components. Item Number: 650-1066
Manufacturer(s)
Zimmer GmbH
Made in
Switzerland

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Zimmer GmbH recalls Biolox Option Taper Sleeve, Type 1 Taper, Standard Neck - Indicated for use in total hip replacement with cemented or no | RecallWatchUSA