Z-1700-2022 Class II Ongoing
FDA device recall Z-1700-2022 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: 37 units.
Recall Details
- Product Type
- Devices
- Report Date
- Sep 14, 2022
- Initiation Date
- Jun 16, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 37 units
Product Description
Various neurology 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) LSRLMNEINTC, 2105181, 870211, 63990989 2) LSRSWRSPNC, 2105251, 861211, 63990357 3) LSRLMNEUROG, 2106161, 845211, 44139500 4) LSRSMHNEURE, 2108101, 793211, 44139500 5) LSRNEURCRANIH, 2108171, 776211, 64123199 6) LSRLMNEUROG, 2110011, 730211, 64316283 7) UINR44M, 2104162, 896211, 64033036 8) TNNE17Y, 2109081, 750211, 64224067 9) SLCR80E, 2104262, 884211, 63986071-006 10) GISP04A, 2104293, 881211, 63985242-006 11) FHNE25Y, 2107083, 811211, 64110740-006 12) BHLA24L, 2108253, 763211, 64205048-006 13) CBAC47F, 2109092, 749211, 64209378-006 14) SLCN72B, 2109161, 741211, 64208359-006 15) BHCR54D, 2104132, 901211, 64072795-006 16) BHCR54D, 2104132, 901211, 64072796-006 17) BHCR54D, 2104132, 901211, 64072273-006 18) BHLM30D, 2105111, 874211, 64062457-006 19) BHCR54D, 2105252, 861211, 64063353-006 20) BHLM30D, 2107091, 819211, 64088774-006 21) BHLM30D, 2107091, 819211, 64088775-006 22) BHLM30D, 2107091, 819211, 64088776-006 23) BHCR54D, 2107161, 810211, 64088824-006 24) BHCR54D, 2107161, 810211, 64088823-006 25) BHLM30D, 2108202, 770211, 64001247-006 26) BHLM30D, 2108202, 770211, 64001248-006 27) BHLM30D, 2108202, 770211, 64001249-006 28) BHLM30D, 2108202, 770211, 64001250-006 29) BHCR54D, 2109022, 757211, 63998620-006 30) BHCR54D, 2109022, 757211, 63998619-006 31) BHCR54D, 2109022, 757211, 63998618-006 32) UMNA22B, 2109292, 728211, 64310294-006 33) DVSP33E, 2104302, 884211, 64064626-006 34) MCSP61F, 2107021, 819211, 64128815-006 35) SJSC27F, 2107091, 813211, 44173743-005 36) SANE32G, 2108091, 784211, 44170921-005 37) MCSP61F, 2108091, 785211, 64138850-006
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1700-2022
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026