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Recall Observatory FDA recall evidence

Device product

KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: SFAR60A

Z-2298-2024

May 15, 2024

Class II

Product summary

Firm
American Contract Systems Inc
Event
Event 94765
Status
Ongoing
Classification
Class II
Quantity
270 units
Official record key
device-enforcement:Z-2298-2024

Official wording

Reason: 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.

Code information: UDI-DI: 00191072167408 LOT#"s: 992241 954241

Distribution pattern: US Nationwide distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.