FDA Device recall Z-0120-2023
MEDLINE ADLT BLOOD CLUTURE COLLECT KIT, Reorder #: DYNDH1245
- FDA Device
- Class II
- ongoing
- Published 2022-11-02
On 2022-11-02 the FDA classified a Class II recall of MEDLINE ADLT BLOOD CLUTURE COLLECT KIT, Reorder #: DYNDH1245 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-0120-2023 |
| 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 ADLT BLOOD CLUTURE COLLECT KIT, Reorder #: DYNDH1245
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)40889942604723 (case), (01)10889942604722 (kit),Lot Number 22FMF306 |
|---|
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-0120-2023%22
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