FDA Device recall Z-0202-2023
MED-RX UROLOGICAL CYSTO/BLADDER IRRIGATION SET, REF 10-4001
- FDA Device
- Class III
- terminated
- Published 2022-11-23
On 2022-11-23 the FDA classified a Class III recall of MED-RX UROLOGICAL CYSTO/BLADDER IRRIGATION SET, REF 10-4001 by Canadian Hospital Specialties, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0202-2023 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2022-08-19 |
| Published | 2022-11-23 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Canadian Hospital Specialties |
| Distribution | n/a |
Product
MED-RX UROLOGICAL CYSTO/BLADDER IRRIGATION SET, REF 10-4001
Reason
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.
Identifiers
| code_info | UDI/DI: 00628725001050, Lot Numbers: 159603, exp 2026-12-01 and 166945, exp 2027-06-01 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0202-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.