Natus Warmette Blanket Cabinet and Warmette Dual Cabinet The Natus… — Class II medical device recall Z-0951-2017
Terminated recall by Natus Manufacturing Limited, reported 2017-01-18, distributed in CA, FL, IL, IN, MA, MS, NC, NJ…. The fuse blows during initial power up or after a period of time. This results in a complete loss of power to
| Recall number | Z-0951-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Natus Manufacturing Limited, GORT, Galway, Ireland |
| Recall initiated | 2016-10-15 |
| Classified | 2017-01-06 |
| Reported by FDA | 2017-01-18 |
| Terminated | 2019-06-24 |
| Distributed | CA, FL, IL, IN, MA, MS, NC, NJ, NY, TX, VA, WA |
| Countries outside the US | CA, CR |
| Quantity | 31 |
| Serial numbers | 10216709, 10216711, 10216713, 10216714, 10218500, 10218501, 10218522, 10218526, 10218528, 10218559, 10218982, 10219214, 10219257, 10219337, 10219338, 10219339, 10219340, 10219387, 10219388, 10219389, 10219390, 10219869, 10219870, 10219871, 10219872 and 6 more |
Product
Natus Warmette Blanket Cabinet and Warmette Dual Cabinet The Natus Warmette Blanket Cabinet is designed to store and warm blankets and hospital linens; while, the Natus Warmette Dual Cabinet is designed to store and warm blankets and hospital linens in one compartment and fluids (irrigation and/or injection) in the other compartment within the storage times and warming temperatures recommended by the manufacturers of those items
Reason for recall
The fuse blows during initial power up or after a period of time. This results in a complete loss of power to the Cabinet and in some cases has resulted in the fuse cover for the power inlet melting slightly.
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-0951-2017. 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.