Cordis POWERFLEX P3 — Class II medical device recall Z-1477-2020
Terminated recall by Cordis Corporation, reported 2020-03-18. Cordis is recalling one (1) lot of POWERFLEX P3 PTA Dilatation Catheter due to the potential for body/shaft vo
| Recall number | Z-1477-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cordis Corporation, Miami Lakes, FL, United States |
| Recall initiated | 2020-01-08 |
| Classified | 2020-03-12 |
| Reported by FDA | 2020-03-18 |
| Terminated | 2023-01-13 |
| Countries outside the US | GB |
| Quantity | 89 units |
| Reason classes | packaging |
| Lot numbers | 82155955 |
| Model numbers | 420-6020S |
| Expiration dates | 2021-06-30 |
Product
Cordis POWERFLEX P3, PTA Dilation Catheter, REF 420-6020S
Reason for recall
Cordis is recalling one (1) lot of POWERFLEX P3 PTA Dilatation Catheter due to the potential for body/shaft voids in the proximal seal area.
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-1477-2020. 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.