Device recall: Omnipod 5 Pods. Includes the below Model/REF Numbers: 1. POD-OMNI-I1-6720. 2. POD-OMNI-I1-6220. 3. OMNI-I1-6729 (10-Pack), OMNI-I1-6720 (Single Pod). 4. OMNI-I1-6220. 5. OMNI-I1-6720. 6. BLE-H1-529 (10-Pack), BLE-H1-520 (Single Pod).
Official structured record identifier: 99034.
Publisher
USA
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- Publisher
- openFDA Device Recalls
- Region
- USA
- Scope
- Regulatory
- Published
- July 8, 2026
- Language
- EN
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Official structured record identifier: 99034.
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Source: openFDA Device Recalls
Scope: Regulatory
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