Data Foundry

Medical device recalls 2025

AMERICAN CONTRACT SYSTEMS — Class II medical device recall Z-2472-2025

Ongoing recall by American Contract Systems Inc, reported 2025-09-03, distributed in IL, LA. During an internal investigation, ACS determined that the rationale for sterilization of certain components wa

Recall numberZ-2472-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmAmerican Contract Systems Inc, Tiffin, OH, United States
Recall initiated2025-07-14
Classified2025-08-28
Reported by FDA2025-09-03
DistributedIL, LA
Quantity588 units
UPC / GTIN / UDI-DI00191072189615, 00191072233004, 00191072233271, 00191072233578, 00191072235411, 00191072235473, 00191072235848
Lot numbers12-7082111, 12-7157111, 12-7309911, 12-7358211, 12-7381311, 12-7400011, 42-7115711, 42-7886011, 42-7897411, 42-7966211, 42-7990911, 42-8134311, 5436801, 70-051243, 70-051850, 70-052358, 70-052715, 70-053042, 70-053457, 70-053862
Model numbersAMAH40N, CCKM67F, HSTH03N, MIAH65B, MPWH01B, SPKA57T, WVAH40H

Product

AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) ANTERIOR HIP PACK, MODEL/ITEM NUMBER AMAH40N; 2)TOTAL KNEE DAN MYER, MODEL/ITEM NUMBER CCKM67F; 3)HIP PROTHESIS PACK, MODEL/ITEM NUMBER HSTH03N; 4)DTC ANTERIOR HIP PACK (PS 209459), MODEL/ITEM NUMBER MIAH65B; 5)DR WHIDD0N TOTAL HIP CPP, MODEL/ITEM NUMBER MPWH01B; 6)KNEE ARTHROSCOPY, MODEL/ITEM NUMBER SPKA57T; 7)ANTERIOR HIP PACK, MODEL/ITEM NUMBER WVAH40H.

Reason for recall

During an internal investigation, ACS determined that the rationale for sterilization of certain components was not justified and therefore, some components are not fit for further sterilization according to ACS procedures. As a result, ACS is unable to confirm product sterilization assurance requirements were met.

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-2472-2025. 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.