Home › BURLINGTON MEDICAL, LLC › F01
F01
BURLINGTON MEDICAL, LLC · Model U3F01-SM · UDI-DI 00840331289596
1
510(k) clearances
5
Adverse events
13
Recalls
80
Facilities
Description
U3F01-SM, MALE(Custom F01: Frontal Apron with Back Strap and Tie Closure .25MM STRATA 300, SM)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-02-11 | Burlington Medical, LLC | Potential for attenuation degradation over time, decreasing the lifespan. |
| 2026-02-11 | Burlington Medical, LLC | Potential for attenuation degradation over time, decreasing the lifespan. |
| 2026-02-11 | Burlington Medical, LLC | Potential for attenuation degradation over time, decreasing the lifespan. |
| 2026-02-11 | Burlington Medical, LLC | Potential for attenuation degradation over time, decreasing the lifespan. |
| 2026-02-11 | Burlington Medical, LLC | Potential for attenuation degradation over time, decreasing the lifespan. |
| 2026-02-11 | Burlington Medical, LLC | Potential for attenuation degradation over time, decreasing the lifespan. |
| 2026-02-11 | Burlington Medical, LLC | Potential for attenuation degradation over time, decreasing the lifespan. |
| 2026-02-11 | Burlington Medical, LLC | Potential for attenuation degradation over time, decreasing the lifespan. |
| 2026-02-11 | Burlington Medical, LLC | Potential for attenuation degradation over time, decreasing the lifespan. |
| 2026-02-11 | Burlington Medical, LLC | Potential for attenuation degradation over time, decreasing the lifespan. |
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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.