FDA Device recall Z-1650-2014
SW-2008 Snuggle Warm Sterile Cardiac Connective Warming Blanket
- FDA Device
- Class II
- terminated
- Published 2014-05-28
On 2014-05-28 the FDA classified a Class II recall of SW-2008 Snuggle Warm Sterile Cardiac Connective Warming Blanket by Smiths Medical Asd, citing the hose could separate from the blanket.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1650-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-04-22 |
| Published | 2014-05-28 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Smiths Medical Asd |
| Distribution | CA, DE, IL, KY, MS, NC, TN, TX, WA, WI |
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
The hose could separate from the blanket.
Identifiers
| code_info | Lot: 1006733, 2474599, 2488138, 2523531, 2536250, 2558180, 2563033, 2564447, 2564448, 2615712 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1650-2014%22
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