Tornier, Inc recalls stryker TORNIER PERFORM HUMERAL SYSTEM - STEMLESS US Anatomic Nucleus, REF DWM003A; anatomic total arthroplasty of the s

Recalled September 25, 2024 · FDA recall Z-3155-2024 · Tornier

Hazard

One lot of Perform Humeral Nucleus may exceed the specification for bacterial endotoxin load (max 20 EU/device). · FDA Class II

Units

5 units

Sold at

US Nationwide distribution in the states of IL, WI, AZ, NV, SD.

Description

One lot of Perform Humeral Nucleus may exceed the specification for bacterial endotoxin load (max 20 EU/device).

Product

stryker TORNIER PERFORM HUMERAL SYSTEM - STEMLESS US Anatomic Nucleus, REF DWM003A; anatomic total arthroplasty of the shoulder

Manufacturer(s)

Tornier, Inc

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