KNEE SCOPE Procedure tray Catalog Number: COKN48L
Reported: July 17, 2024 Initiated: May 15, 2024 #Z-2287-2024
Product Description
KNEE SCOPE Procedure tray Catalog Number: COKN48L
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
- 36 units
- Distribution
- US Nationwide distribution.
- Location
- Tiffin, OH
Frequently Asked Questions
What product was recalled? ▼
KNEE SCOPE Procedure tray Catalog Number: COKN48L. Recalled by American Contract Systems Inc. Units affected: 36 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-2287-2024.
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