MEDLINE BLOOD CULTURE BOTTLE KIT — Class II medical device recall Z-0964-2024
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-02-07, distributed nationwide. Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Cu
| Recall number | Z-0964-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2023-12-21 |
| Classified | 2024-02-01 |
| Reported by FDA | 2024-02-07 |
| Distributed | Nationwide (US) |
| Quantity | 775 units |
| UPC / GTIN / UDI-DI | 10195327239848, 40195327239849 |
| Lot numbers | 23JBM366 |
Product
MEDLINE BLOOD CULTURE BOTTLE KIT, Reorder Number DYNDH1738A
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0964-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.