Recall Z-2471-2025— American Contract Systems Inc
Class II · Ongoing
Class II FDA medical device recall by American Contract Systems Inc, initiated 2025-07-14. FDA's recall record names no specific 510(k) clearance for this event. Product: AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) ROBOT HYST PACK, MODEL/ITEM NUMBER GRRB10E; 2) VAG HYST PACK, MODEL/ITEM NUMBER SPVH62P.. Reason: 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..
- Recalling firm
- American Contract Systems Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-07-14
- Firm location
- Tiffin, OH, United States
Product description
AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) ROBOT HYST PACK, MODEL/ITEM NUMBER GRRB10E; 2) VAG HYST PACK, MODEL/ITEM NUMBER SPVH62P.
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.