Z-0106-2023 Class II Terminated
FDA device recall Z-0106-2023 was initiated by MEDLINE INDUSTRIES, LP - Northfield on Sep 7, 2022 and is designated Class II. Reason for recall: One lot of chest tube insertion trays, containing a silk suture component that is restricted to 1 cycle of sterilization, was processed though 2 cycles. The recall status is terminated (terminated Mar 4, 2026). Affected quantity: 18 kits.
Recall Details
- Product Type
- Devices
- Report Date
- Oct 26, 2022
- Initiation Date
- Sep 7, 2022
- Termination Date
- Mar 4, 2026
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 18 kits
Product Description
CENTURION SnagFree Chest Tube insertion Tray, Reorder CHT545
Reason for Recall
One lot of chest tube insertion trays, containing a silk suture component that is restricted to 1 cycle of sterilization, was processed though 2 cycles.
Distribution Pattern
US Nationwide distribution in the states of CA and TX.
Code Information
UDI/DI 20653160222979, Lot Code 2022050690
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0106-2023
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026