KNEE ARTHROSCOPY-Procedure Kit Catalog Number: SLAR14G
Reported: July 17, 2024 Initiated: May 15, 2024 #Z-2301-2024
Product Description
KNEE ARTHROSCOPY-Procedure Kit Catalog Number: SLAR14G
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
- Recalling Firm
- American Contract Systems Inc
- Units Affected
- 28 units
- Distribution
- US Nationwide distribution.
- Location
- Tiffin, OH
Frequently Asked Questions
What product was recalled? ▼
KNEE ARTHROSCOPY-Procedure Kit Catalog Number: SLAR14G. Recalled by American Contract Systems Inc. Units affected: 28 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-2301-2024.
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