Z-1695-2022 Class II Ongoing
FDA device recall Z-1695-2022 was initiated by American Contract Systems, Inc. on Jun 16, 2022 and is designated Class II. Reason for recall: Product was exposed to multiple sterilization cycles without validation for multiple exposures. The recall status is ongoing. Affected quantity: 21 units.
Recall Details
- Product Type
- Devices
- Report Date
- Sep 14, 2022
- Initiation Date
- Jun 16, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 21 units
Product Description
Various Cysto Packs
Reason for Recall
Product was exposed to multiple sterilization cycles without validation for multiple exposures.
Distribution Pattern
Distribution within the United States to health systems and distributors in AZ, FL, IA, IL, MA, MN, MO, OH, NE, PA, RI, SD, and TX
Code Information
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
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1695-2022
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 24, 2026