Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-3231-2024Class II

Day Surgery General Pack, FHGE18T; Medical convenience kit

American Contract Systems, Inc. / initiated 2024-08-07 / Open, Classified / root cause: sterility

American Contract Systems, Inc. began a recall of Day Surgery General Pack, FHGE18T; Medical convenience kit on . FDA classified it as Class II and gives the reason as "ACS identified that due to an inoperable chart recorder, humidity readings were out-of-specification in one of the controlled environment areas. As a result, ACS is unable to confirm product sterilization assurance...". As of , the recall status on record is Open, Classified, and MDM tags the root cause as sterility.

Recall record

Recall number
Z-3231-2024
Classification
Class II
Status
Open, Classified
Initiated
Posted
Recalling firm
American Contract Systems, Inc.
Product
Day Surgery General Pack, FHGE18T; Medical convenience kit
Product code
LRO General Surgery Tray
Reason for recall
ACS identified that due to an inoperable chart recorder, humidity readings were out-of-specification in one of the controlled environment areas. As a result, ACS is unable to confirm product sterilization assurance requirements were met.
Root cause tag
sterility
FDA root cause
Under Investigation by firm
Action
Owens & Minor issued an URGENT: MEDICAL DEVICE FIELD CORRECTION to its consignees on 08/07/2024 via email. The notice explained the issue, potential risk to health, and requested the following actions be taken: " -Please review your inventory, and segregate and quarantine all affected Trays. If any of the affected trays identified above were further distributed, please ensure all end-users are appropriately notified and maintain records of effectiveness. - Owens & Minor issued an URGENT: MEDICAL DEVICE FIELD CORRECTION to its consignees on 08/07/2024 via email. The notice explained the issue, potential risk to health, and requested the following actions be taken: " Please review your inventory, and segregate and quarantine all affected Trays. If any of the affected trays identified above were further distributed, please ensure all end-users are appropriately notified and maintain records of effectiveness. - Discard all affected kits and document on the enclosed Response Form."
Quantity in commerce
280 units
Distribution
US Nationwide distribution in the states of MO, MN, MA, OH, NE.
Product codes and lots
UDI-DI: 00191072210517; Lot: 2405131; Exp: 05/13/2025

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-3231-2024
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-3226-2024Class IIOngoingVoluntary: Firm initiated
Z-3227-2024Class IIOngoingVoluntary: Firm initiated
Z-3228-2024Class IIOngoingVoluntary: Firm initiated
Z-3229-2024Class IIOngoingVoluntary: Firm initiated
Z-3230-2024Class IIOngoingVoluntary: Firm initiated
Z-3231-2024Class IIOngoingVoluntary: Firm initiated
Z-3232-2024Class IIOngoingVoluntary: Firm initiated
Z-3233-2024Class IIOngoingVoluntary: Firm initiated
Z-3234-2024Class IIOngoingVoluntary: Firm initiated
Z-3235-2024Class IIOngoingVoluntary: Firm initiated
Z-3236-2024Class IIOngoingVoluntary: Firm initiated
Z-3237-2024Class IIOngoingVoluntary: Firm initiated
Z-3238-2024Class IIOngoingVoluntary: Firm initiated
Z-3239-2024Class IIOngoingVoluntary: Firm initiated
Z-3240-2024Class IIOngoingVoluntary: Firm initiated
Z-3241-2024Class IIOngoingVoluntary: Firm initiated
Z-3242-2024Class IIOngoingVoluntary: Firm initiated
Z-3243-2024Class IIOngoingVoluntary: Firm initiated
Z-3244-2024Class IIOngoingVoluntary: Firm initiated