Home › Encompass Group, L.L.C. › Thermoflect
Thermoflect
Encompass Group, L.L.C. · Model 5145-500 · UDI-DI 30612899003188
FME
Prescription
5
510(k) clearances
8
Adverse events (1 deaths)
1
Recalls
237
Facilities
Description
THERMOFLECT GOWN, XL, 25EA TS THERMOFLECT GOWN, STANDARD, SILVER/BLUE, 5/BG, 5 BG/CS NW
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2009-12-23 | Encompass Group LLC | The products are not compatible for use in the Magnetic Resonance Imaging (MRI) environment. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
