MEDLINE PHERIPHERAL BLOOD CULTURE DRAW — Class II medical device recall Z-0121-2023
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2022-11-02, distributed nationwide. Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a comp
| Recall number | Z-0121-2023 |
|---|---|
| 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 | 2022-09-09 |
| Classified | 2022-10-21 |
| Reported by FDA | 2022-11-02 |
| Distributed | Nationwide (US) |
| Quantity | 1,020 kits |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 10193489402810, 40193489402811 |
| Lot numbers | 22FMF307 |
Product
MEDLINE PHERIPHERAL BLOOD CULTURE DRAW, Reorder #: DYNDH1561
Reason for recall
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.
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-0121-2023. 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.