SW-2008 Snuggle Warm Sterile Cardiac Connective Warming Blanket — Class II medical device recall Z-1650-2014
Terminated recall by Smiths Medical ASD, Inc., reported 2014-05-28, distributed in CA, IL, KY, MS, NC, TN, TX, WA…. The hose could separate from the blanket.
| Recall number | Z-1650-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smiths Medical ASD, Inc., Rockland, MA, United States |
| Recall initiated | 2014-04-22 |
| Classified | 2014-05-22 |
| Reported by FDA | 2014-05-28 |
| Terminated | 2015-02-27 |
| Distributed | CA, IL, KY, MS, NC, TN, TX, WA, WI |
| Quantity | 2,120 devices |
| Lot numbers | 1006733, 2474599, 2488138, 2523531, 2536250, 2558180, 2563033, 2564447, 2564448, 2615712 |
Product
SW-2008 Snuggle Warm Sterile Cardiac Connective Warming Blanket; used with the Equator Convective Warmer, are intended for thermal regulation of a patient's temperture and are designed to prevent hypothermia and/ or reduce cold discomfort during and after surgical procedures.
Reason for recall
The hose could separate from the blanket.
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-1650-2014. 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.