Monoject — Class II medical device recall Z-0112-2024
Ongoing recall by Cardinal Health 200, LLC, reported 2023-10-25, distributed nationwide. Syringe contains conical tip that is not compatible with certain needleless IV connector(s).
| Recall number | Z-0112-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cardinal Health 200, LLC, Waukegan, IL, United States |
| Recall initiated | 2023-09-13 |
| Classified | 2023-10-13 |
| Reported by FDA | 2023-10-25 |
| Distributed | Nationwide (US) |
| UPC / GTIN / UDI-DI | 10192253034530, 20192253034537, 50192253034538 |
| Lot numbers | 221201, 221202, 221203, 230201, 230202, 230203, 230204, 230205, 230601 |
Product
Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, Model Number/Product Code: 1180100777
Reason for recall
Syringe contains conical tip that is not compatible with certain needleless IV connector(s).
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-0112-2024. 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.