Z-0202-2023 Class III Terminated
FDA device recall Z-0202-2023 was initiated by Canadian Hospital Specialties on August 19, 2022 and is designated Class III. Reason for recall: Some of the labels of the kits for product code 10-4001 in the specified lots have an illegible barcode which prevents successful scanning of the package. The recall status is terminated (terminated March 20, 2023). Affected quantity: 9100 units.
Recall Details
- Product Type
- Devices
- Report Date
- November 23, 2022
- Initiation Date
- August 19, 2022
- Termination Date
- March 20, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 9100 units
Product Description
MED-RX UROLOGICAL CYSTO/BLADDER IRRIGATION SET, REF 10-4001
Reason for Recall
Some of the labels of the kits for product code 10-4001 in the specified lots have an illegible barcode which prevents successful scanning of the package.
Distribution Pattern
US
Code Information
UDI/DI: 00628725001050, Lot Numbers: 159603, exp 2026-12-01 and 166945, exp 2027-06-01