FDA Device recall Z-2548-2017
SCHRITTMACHER ANGIO X3
- FDA Device
- Class II
- terminated
- Published 2017-06-21
On 2017-06-21 the FDA classified a Class II recall of SCHRITTMACHER ANGIO X3 by Medtronic, citing potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2548-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-05-03 |
| Published | 2017-06-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Medtronic |
| Distribution | US |
Product
SCHRITTMACHER ANGIO X3; Item Number: 4045255423347
Reason
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
Identifiers
| code_info | 228111X |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2548-2017%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.