FDA Device recall Z-2522-2024
American Contract Systems Cataract Pack convenience kit
- FDA Device
- Class II
- ongoing
- Published 2024-08-14
On 2024-08-14 the FDA classified a Class II recall of American Contract Systems Cataract Pack convenience kit by American Contract Systems, citing product released with insufficient aeration time impacting the kits sterilized on the same cycle or in the same aeration chamber.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2522-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-05-06 |
| Published | 2024-08-14 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | American Contract Systems |
| Distribution | US |
Product
American Contract Systems Cataract Pack convenience kit
Reason
Product released with insufficient aeration time impacting the kits sterilized on the same cycle or in the same aeration chamber
Identifiers
| code_info | UDI-DI 00191072188762; Lot 988241; Exp. Date 1/12/2025. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2522-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.