IR1200 — Class II medical device recall Z-0005-2013
Terminated recall by Animas Corporation, reported 2012-10-10, distributed nationwide. Wear of the keypad that may lead to damage such as tearing or peeling of the edge of the keypad from the pump.
| Recall number | Z-0005-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Animas Corporation, West Chester, PA, United States |
| Recall initiated | 2012-07-16 |
| Classified | 2012-10-02 |
| Reported by FDA | 2012-10-10 |
| Terminated | 2014-01-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, CA, CZ, DE, ES, FI, FR, GB, HU, IL, IT, MX, NZ |
| Quantity | 236,470 |
| Model numbers | 100200-00, 100201-00, 100202-00, 100250-00, 100251-00, 100252-00, 100380-00, 100381-00, 100382-00, 100384-00, 100385-00, 100430-00, 100431-00, 100432-00, 100434-00, 100435-00, 101370-00, 101371-00, 101372-00, 101374-00, 101375-00, 101420-00, 101420-98, 101421-00, 101421-98 and 6 more |
Product
IR1200, IR1250(IR1200 Plus), 2020 and One Touch(R) Ping(R) Insulin Pump glucose management system. The device is intended to deliver insulin therapy.
Reason for recall
Wear of the keypad that may lead to damage such as tearing or peeling of the edge of the keypad from the pump.
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-0005-2013. 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.