FDA Device recall Z-0250-2020
Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use
- FDA Device
- Class II
- terminated
- Published 2019-11-06
On 2019-11-06 the FDA classified a Class II recall of Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use by Cordis, citing product was manufactured utilizing an expired inner body.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0250-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-10-04 |
| Published | 2019-11-06 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Cordis |
| Distribution | AL, AZ, FL, MN, MO |
Product
Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.
Reason
Product was manufactured utilizing an expired inner body.
Identifiers
| code_info | Catalog Number: 4171460S; Lot Number: 82169860; Expiry Date: 10/31/2020 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0250-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.