CareFusion MaxPlus Clear Needleless Connector — Class II medical device recall Z-0049-2020
Terminated recall by Becton Dickinson & Company, reported 2019-10-16, distributed nationwide. After disconnection of a luer, the valve of the connector remains recessed; not fully closing, either temporar
| Recall number | Z-0049-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Company, Franklin Lakes, NJ, United States |
| Recall initiated | 2019-05-02 |
| Classified | 2019-10-07 |
| Reported by FDA | 2019-10-16 |
| Terminated | 2021-11-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 115,200 |
| UPC / GTIN / UDI-DI | 10885403223228 |
| Lot numbers | 18085990 |
| Model numbers | MP1000-C |
| Expiration dates | 2023-08-15 |
Product
CareFusion MaxPlus Clear Needleless Connector. Intended for Positive Displacement Connector for needleless access to the IV line and/or IV catheter during IV therapy Cat. No. MP1000-C
Reason for recall
After disconnection of a luer, the valve of the connector remains recessed; not fully closing, either temporarily or permanently. The risks of blood loss and air embolism exist if the valve remains permanently open and goes undetected, especially in the neonate population.
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-0049-2020. 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.