FDA Device recall Z-0124-2023
MEDLINE PRE-OP CHG BATHING KIT Reorder #: P164756
- FDA Device
- Class II
- ongoing
- Published 2022-11-02
On 2022-11-02 the FDA classified a Class II recall of MEDLINE PRE-OP CHG BATHING KIT Reorder #: P164756 by Medline Industries Northfield, citing adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0124-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-09-09 |
| Published | 2022-11-02 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
MEDLINE PRE-OP CHG BATHING KIT Reorder #: P164756
Reason
Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and Bactec bottle plastic both have an expiration date that does not match the date listed on the kit.
Identifiers
| code_info | UDI/DI: (01)40888277983824 (case), (01)10888277983823 (kit), Lot Numbers: 22EMI516, 22DMG491 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0124-2023%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.