PlainRecalls
FDA Devices Moderate Class II Ongoing

TOTAL KNEE - 247546 - Procedure tray Catalog Number: BFTK01AA

Reported: July 17, 2024 Initiated: May 15, 2024 #Z-2278-2024

Product Description

TOTAL KNEE - 247546 - Procedure tray Catalog Number: BFTK01AA

Reason for Recall

Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.

Details

Units Affected
N/A
Distribution
US Nationwide distribution.
Location
Tiffin, OH

Frequently Asked Questions

What product was recalled?
TOTAL KNEE - 247546 - Procedure tray Catalog Number: BFTK01AA. Recalled by American Contract Systems Inc. Units affected: N/A.
Why was this product recalled?
Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 17, 2024. Severity: Moderate. Recall number: Z-2278-2024.