Home › Flow X Ray Corporation › Special Procedure Apron, Standard Lead, XX Large
Special Procedure Apron, Standard Lead, XX Large
Flow X Ray Corporation · Model 67090-36 · UDI-DI 00843696130862
1
510(k) clearances
5
Adverse events
13
Recalls
80
Facilities
Description
Special Procedure Apron 0.5 mm front protection, 0.25 mm back protection, 25" x 42", Xtra Xtra Large, Hunter Green
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.