FDA Device recall Z-1695-2022
Various Cysto Packs
- FDA Device
- Class II
- ongoing
- Published 2022-09-14
On 2022-09-14 the FDA classified a Class II recall of Various Cysto Packs by American Contract Systems, citing product was exposed to multiple sterilization cycles without validation for multiple exposures.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1695-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-06-16 |
| Published | 2022-09-14 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | American Contract Systems |
| Distribution | AZ, FL, IA, IL, MA, MN, MO, NE, OH, PA, RI, SD, TX |
Product
Various Cysto Packs
Reason
Product was exposed to multiple sterilization cycles without validation for multiple exposures.
Identifiers
| code_info | Tray Number, Sterilization Lot, Lot Number, Bag Serial Number 1) LSRCFHCYTURC, 2105051, 883211, 15142078 2) LSRCFHCYT…Tray Number, Sterilization Lot, Lot Number, Bag Serial Number 1) LSRCFHCYTURC, 2105051, 883211, 15142078 2) LSRCFHCYTURC, 2106092, 853211, 44251068 3) LSRCYSTOTURF, 2106181, 834211, 44251068 4) LSRCYSTOTURF, 2108251, 775211, 44376072 5) JECY99B, 2105182, 862211, 44108484-005 6) BHCY71H, 2107011, 819211, 44247051-005 7) SLCY61, 2108111, 777211, 15093750-004 8) BHCY31D, 2107161, 810211, 44228702-005 9) BHCY31D, 2107161, 810211, 44228704-005 10) BHCY31D, 2107161, 810211, 44228703-005 11) BHCY31D, 2109032, 763211, 44333133-005 12) BHCY31D, 2109032, 763211, 44333132-005 13) BHCY31D, 2109032, 763211, 44333131-005 14) BHCY31D, 2109032, 763211, 44333300-005 15) BHCY31D, 2109032, 763211, 44333398-005 16) BHCY31D, 2110051, 726211, 44351428-005 17) BHCY31D, 2110051, 726211, 44351427-005 18) BHCY31D, 2110051, 726211, 44351426-005 19) BHCY31D, 2110051, 726211, 44351425-005 20) UTCY45M, 2104231, 890211, 44175283-005 21) FRCY56D, 2105121, 869211, 44173978-005 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1695-2022%22
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