PlainRecalls
FDA Devices Moderate Class II Ongoing

BPKN15C KNEE BASIN PACK BHS- Procedure tray Catalog Number: BPKN15C

Reported: July 17, 2024 Initiated: May 15, 2024 #Z-2284-2024

Product Description

BPKN15C KNEE BASIN PACK BHS- Procedure tray Catalog Number: BPKN15C

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
552 units
Distribution
US Nationwide distribution.
Location
Tiffin, OH

Frequently Asked Questions

What product was recalled?
BPKN15C KNEE BASIN PACK BHS- Procedure tray Catalog Number: BPKN15C. Recalled by American Contract Systems Inc. Units affected: 552 units.
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-2284-2024.