Insulet Corporation
4
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-04-22 to 2026-07-08
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-07-08 | FDA Device | FDA Recall: Omnipod 5 Pods. Includes the below Model/REF Numbers: 1. POD-OMNI-I1-6720. 2. POD-OMNI-I1-622 | Insulet Corporation | Class I | N/A |
| 2026-07-08 | FDA Device | FDA Recall: Omnipod DASH Pod. Includes the below Model/REF Numbers: 1. POD-BLE-I1-525 (5-Pack), POD-BLE-I1-5 | Insulet Corporation | Class I | N/A |
| 2026-07-08 | FDA Device | FDA Recall: Omnipod (Eros) Pod. Includes the below Model/REF Numbers: 1. POD-ZXP425 (10 Pack), POD- ZXP420 ( | Insulet Corporation | Class I | N/A |
| 2026-04-22 | FDA Device | FDA Recall: Omnipod 5 Pods. Model/Catalog number: PT-001662 ASM 5PK Pod STRL OPS G6G7 | Insulet Corporation | Class I | N/A |