RecallWatchUSA

Home / Recalls / Medical Devices

Howmedica Osteonics Corp. recalls SCORPIO RECESSED PATELLA-Intended for knee repalcment Part Number: 3044-0032

Recalled February 7, 2024 · FDA recall Z-0872-2024 · Howmedica Osteonics

Hazard
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties. · FDA Class II
Units
70 units US
Sold at
Nationwide Foreign: Argentina, Australia, Brazil, Canada, Chile, China, Columbia, India, Japan, Korea, Latin America, Mexico, Poland, Sweden, Switzerland, Taiwan, UK, & Venlo (Netherlands). ***Updated 1/25/24*** Foreign distribution added: Austria, Finland, Germany, Ireland, Hong Kong, New Zealand, Norway, and Spain.

Description

Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

Product
SCORPIO RECESSED PATELLA-Intended for knee repalcment Part Number: 3044-0032
Manufacturer(s)
Howmedica Osteonics Corp.

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

Howmedica Osteonics Corp. recalls SCORPIO RECESSED PATELLA-Intended for knee repalcment Part Number: 3044-0032 | RecallWatchUSA