AMSCO¿ Warming Cabinet — Class II medical device recall Z-0603-2016
Terminated recall by Steris Corporation, reported 2016-01-13, distributed nationwide. The firm discovered that information printed on the quick reference magnet is incorrect; specifically, Fahrenh
| Recall number | Z-0603-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Steris Corporation, Mentor, OH, United States |
| Recall initiated | 2015-11-20 |
| Classified | 2016-01-06 |
| Reported by FDA | 2016-01-13 |
| Terminated | 2016-10-27 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BH, CA, CN, CO, CR, ES, FR, HK, ID, IL, IN, KR, KW, LB, MX, PA, PE, SA, SG, TH, TR, TW, VN |
| Quantity | 2,319 units |
| Serial numbers | 0428014026, 0432115014 |
Product
AMSCO¿ Warming Cabinet. Manufactured by: STERIS Corporation To raise the temperature of blankets, linens and sterile surgical IV/irrigation solutions to an acceptable level for various surgical, obstetrical, emergency, critical care and other healthcare applications.
Reason for recall
The firm discovered that information printed on the quick reference magnet is incorrect; specifically, Fahrenheit to Celsius temperature conversions and the default Warming Cabinet temperature.
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-0603-2016. 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.