PICC Line Accessory Kit CVI4285 — Class II medical device recall Z-0075-2020
Terminated recall by Centurion Medical Products Corporation, reported 2019-10-16, distributed nationwide. Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer
| Recall number | Z-0075-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Centurion Medical Products Corporation, Williamston, MI, United States |
| Recall initiated | 2019-04-24 |
| Classified | 2019-10-09 |
| Reported by FDA | 2019-10-16 |
| Terminated | 2020-04-03 |
| Distributed | Nationwide (US) |
| Quantity | 181,965 |
Product
PICC Line Accessory Kit CVI4285
Reason for recall
Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
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-0075-2020. 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.