PORT ACCESS INFUSION KIT — Class II medical device recall Z-0256-2020
Terminated recall by Centurion Medical Products Corporation, reported 2019-11-06, distributed in IL. Supplier initiated recall of the GRIPPER Needles
| Recall number | Z-0256-2020 |
|---|---|
| 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 | 2019-07-15 |
| Classified | 2019-10-31 |
| Reported by FDA | 2019-11-06 |
| Terminated | 2020-08-31 |
| Distributed | IL |
| Quantity | 200 kits |
| Lot numbers | 2019060390 |
Product
PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817
Reason for recall
Supplier initiated recall of the GRIPPER Needles
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-0256-2020. 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.