PlainRecalls
FDA Devices Moderate Class II Ongoing

AHAR50K STANDARD ARTHROSCOPY PACK - 291852. Procedure tray Catalog Number: AHAR50K

Reported: July 17, 2024 Initiated: May 15, 2024 #Z-2274-2024

Product Description

AHAR50K STANDARD ARTHROSCOPY PACK - 291852. Procedure tray Catalog Number: AHAR50K

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
345 units
Distribution
US Nationwide distribution.
Location
Tiffin, OH

Frequently Asked Questions

What product was recalled?
AHAR50K STANDARD ARTHROSCOPY PACK - 291852. Procedure tray Catalog Number: AHAR50K. Recalled by American Contract Systems Inc. Units affected: 345 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-2274-2024.