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FDA Medical Device Recalls (openFDA)

American Contract Systems Inc: THORACIC PACK , Model No UTTC82Y UTTC82AA-01

Recall number
Z-1361-2025
Recalling firm
American Contract Systems Inc
Product
THORACIC PACK , Model No UTTC82Y UTTC82AA-01
Status
Open, Classified
Initiated
2025-02-06
Posted
2025-03-14
Terminated
not on file
Reason
ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
Root cause
Process control
Action
The affected distributor was notified via email on 2/16/25, and an updated letter was provided on 2/18/25. The distributor was instructed to notify their end users. Customers were provided with a list of impacted components which are included in the affected trays. Customers were provided with a labeling template and instructed to add warning labels to affected procedure trays to ensure the affected components are discarded.
Quantity
40 kits
Distribution
US Nationwide distribution in the state of OH.
Lot, serial or model codes
UDI-DI 00191072147332 Lots 954241 921241 889241 70-051283 70-052001 70-052096 70-053233
510(k) numbers
not on file
PMA numbers
not on file
Product code
OEZ
Firm FEI
3008492337
Firm city
Tiffin
Firm state
OH
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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