Data Foundry

Medical device recalls 2025

Medical convenience kits Item Number/Description HSLM53AB SPINE PACK… — Class II medical device recall Z-0183-2026

Ongoing recall by American Contract Systems Inc., reported 2025-10-22, distributed nationwide. Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the init

Recall numberZ-0183-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmAmerican Contract Systems Inc., Grimes, IA, United States
Recall initiated2025-09-04
Classified2025-10-16
Reported by FDA2025-10-22
DistributedNationwide (US)
Quantity32,433 total
Reason classeschemical contamination
UPC / GTIN / UDI-DI00191072210333, 00191072210340, 00191072214089, 00191072214423, 00191072217400, 00191072224095, 00191072227843, 00191072228536, 00191072231512, 00191072232076
Lot numbers8024911, 8028211, 8056311, 8061111, 8067511, 8105511, 8192111, 8361111, 8382011, 8441711
Serial numbers17621919, 68055493, 68138618, 68138767, 68140374, 68154067, 68195596, 68576542, 68680026, ANPP15AR, HSLM53AB, MILM82A, RCNA47B, SFLM54AB, UDLM94AA, UILM77AU, UINR44P, UISH15AV

Product

Medical convenience kits Item Number/Description HSLM53AB SPINE PACK MILM82A DTC LAMINECTOMY PACK (PS 209475) RCNA47B NEURO ANGIO 0246971 SFLM54AB LAMINECTOMY PACK - 219659 UDLM94AA LAMINECTOMY PACK - 206064 UILM77AU LAMINECTOMY (PS 039500) UINR44P NEURO IR PERIPHERAL (PS 64405) UISH15AV SHUNT PACK (PS 039360)

Reason for recall

Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, product quality, safety, and effectiveness cannot be confirmed for product that was re-gassed.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0183-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.