FDA Device recall Z-0965-2024
MEDLINE BLOOD CULTURE COLLECTION KIT, Reorder Number DYNDH1714A
- FDA Device
- Class II
- ongoing
- Published 2024-02-07
On 2024-02-07 the FDA classified a Class II recall of MEDLINE BLOOD CULTURE COLLECTION KIT, Reorder Number DYNDH1714A by Medline Industries Northfield, citing medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0965-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-12-21 |
| Published | 2024-02-07 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
MEDLINE BLOOD CULTURE COLLECTION KIT, Reorder Number DYNDH1714A
Reason
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
Identifiers
| code_info | UDI/DI 40195327347551 (case), 10195327347550 (unit), Lot Numbers: 23KBC138 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0965-2024%22
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