ACS UICL44PRecalls & reported problems
American Contract Systems, Inc. · ADULT CENTRAL LINE INSERTION SUPPLY KIT · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Sep 4, 2025Open, Classified
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.
Z-0177-2026 · Root cause: Nonconforming Material/Component · FDA record ↗
Other Central venous catheter tray devices
- Medline Industries, Inc. DYNJ70141MBMedline Industries, Inc. · Central venous catheter tray4 recalls1 report
- Medline Industries, Inc. DYNJ70152MBMedline Industries, Inc. · Central venous catheter tray4 recalls0 reports
- Medline Industries, Inc. DYNJ63199AMedline Industries, Inc. · Central venous catheter tray3 recalls0 reports
- Medline Industries, Inc. DYNJ80643Medline Industries, Inc. · Central venous catheter tray3 recalls0 reports
- Medline Industries, Inc. DYNJ55546DMedline Industries, Inc. · Central venous catheter tray3 recalls0 reports
- Medline Industries, Inc. DYNJ66271BMedline Industries, Inc. · Central venous catheter tray3 recalls0 reports
- Medline Industries, Inc. DYNJ68037CMedline Industries, Inc. · Central venous catheter tray2 recalls1 report
- Medline Industries, Inc. ACC010487Medline Industries, Inc. · Central venous catheter tray2 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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