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Aesculap Implant Systems LLC recalls Aesculap Surgical Needle, straight, 3 1/2", (90 mm), 13GA, width: 2,400 mm, non-sterile, reusable Article Number: MD610
Recalled July 26, 2023 · FDA recall Z-2146-2023 · Aesculap Implant Systems
Hazard
Incorrect product code marked on the product, etched with product code MD611, however; the correct product code is MD610. · FDA Class II
Units
7 units
Sold at
US Nationwide distribution in the states of DC, MO, PA, TX.
Description
Incorrect product code marked on the product, etched with product code MD611, however; the correct product code is MD610.
Product
Aesculap Surgical Needle, straight, 3 1/2", (90 mm), 13GA, width: 2,400 mm, non-sterile, reusable Article Number: MD610
Manufacturer(s)
Aesculap Implant Systems LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →