Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-0177-2026Class II

Medical convenience kits Item Number/Description UICL44P ADULT CENTRAL LINE INSERTION SUPPLY KIT UICL44R...

American Contract Systems, Inc. / initiated 2025-09-04 / Open, Classified / root cause: manufacturing process

American Contract Systems Inc. began a recall of Medical convenience kits Item Number/Description UICL44P ADULT CENTRAL LINE INSERTION SUPPLY KIT UICL44R ADULT CENTRAL LINE INSERTION SUPPLY KIT on . FDA classified it as Class II and gives the reason as "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...". As of , the recall status on record is Open, Classified, and MDM tags the root cause as manufacturing process.

Recall record

Recall number
Z-0177-2026
Classification
Class II
Status
Open, Classified
Initiated
Posted
Recalling firm
American Contract Systems, Inc.
Product
Medical convenience kits Item Number/Description UICL44P ADULT CENTRAL LINE INSERTION SUPPLY KIT UICL44R ADULT CENTRAL LINE INSERTION SUPPLY KIT
Product code
OFF Central Venous Catheter Tray
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.
Root cause tag
manufacturing process
FDA root cause
Nonconforming Material/Component
Action
Firm notified affected distributors who received affected product via email on 9/4/25. An updated letter was provided on 9/9/25, which better clarified product codes and impacted lot numbers and bag serial numbers. Consignees were instructed to immediately discontinue use and discard impacted trays. Distribution partners were provided with a customer letter for further distribution to end users.
Quantity in commerce
32,433 total
Distribution
US Nationwide distribution in the states of SD, IA, MN, WA, IL.
Product codes and lots
UICL44P UDI-DI 191072194268 Lot 8003911 Bag serial number N/A; UICL44R UDI-DI 191072234018 Lot 8317711 Bag serial number 68244081 * If bag serial number is listed as "n/a", then entire lot is affected

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-0177-2026
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-0170-2026Class IIOngoingVoluntary: Firm initiated
Z-0171-2026Class IIOngoingVoluntary: Firm initiated
Z-0172-2026Class IIOngoingVoluntary: Firm initiated
Z-0173-2026Class IIOngoingVoluntary: Firm initiated
Z-0174-2026Class IIOngoingVoluntary: Firm initiated
Z-0175-2026Class IIOngoingVoluntary: Firm initiated
Z-0176-2026Class IIOngoingVoluntary: Firm initiated
Z-0177-2026Class IIOngoingVoluntary: Firm initiated
Z-0178-2026Class IIOngoingVoluntary: Firm initiated
Z-0179-2026Class IIOngoingVoluntary: Firm initiated
Z-0180-2026Class IIOngoingVoluntary: Firm initiated
Z-0181-2026Class IIOngoingVoluntary: Firm initiated
Z-0182-2026Class IIOngoingVoluntary: Firm initiated
Z-0183-2026Class IIOngoingVoluntary: Firm initiated
Z-0184-2026Class IIOngoingVoluntary: Firm initiated
Z-0185-2026Class IIOngoingVoluntary: Firm initiated
Z-0186-2026Class IIOngoingVoluntary: Firm initiated
Z-0187-2026Class IIOngoingVoluntary: Firm initiated