FDA Device recall Z-0312-2024
CENTRAL LINE BLOOD CULTURE DRA, REF DYNDH1562
- FDA Device
- Class II
- ongoing
- Published 2023-11-22
On 2023-11-22 the FDA classified a Class II recall of CENTRAL LINE BLOOD CULTURE DRA, REF DYNDH1562 by Medline Industries Northfield, citing this recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0312-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-11-01 |
| Published | 2023-11-22 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
CENTRAL LINE BLOOD CULTURE DRA, REF DYNDH1562
Reason
This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.
Identifiers
| code_info | UDI/DI 40193489402446 (case), 10193489402445 (unit): Lot Numbers: 23DMF156, 23CMH030, 23CMD955 |
|---|
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-0312-2024%22
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