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FDA Medical Device Recalls (openFDA)

American Contract Systems Inc: LACERATION TRAY , Model No SGLA07A SGLA07B-01 SGLA07B-02 SGLA07B

Recall number
Z-1349-2025
Recalling firm
American Contract Systems Inc
Product
LACERATION TRAY , Model No SGLA07A SGLA07B-01 SGLA07B-02 SGLA07B
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
690 kits
Distribution
US Nationwide distribution in the state of OH.
Lot, serial or model codes
UDI-DI 00191072135063 00191072223715 Lots 899241 70-050880 70-051697 70-052161 70-052662
510(k) numbers
not on file
PMA numbers
not on file
Product code
LRO
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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