American Contract Systems, Inc.: Device Recall

Recall #Z-3235-2024 · 08/07/2024

Class II: Risk

Recall Details

Recall Number
Z-3235-2024
Classification
Class II
Product Type
Device
Recalling Firm
American Contract Systems, Inc.
Status
Ongoing
Date Initiated
08/07/2024
Location
Kansas City, MO, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1 unit

Reason for Recall

ACS identified that due to an inoperable chart recorder, humidity readings were out-of-specification in one of the controlled environment areas. As a result, ACS is unable to confirm product sterilization assurance requirements were met.

Product Description

IR Procedure Pack, CEAT19W; Medical convenience kit

Distribution Pattern

US Nationwide distribution in the states of MO, MN, MA, OH, NE.

Other Recalls by American Contract Systems, Inc.

View all recalls by American Contract Systems, Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.