Home › Flow X Ray Corporation › Front Closing Special Procedure, Lead, Small
Front Closing Special Procedure, Lead, Small
Flow X Ray Corporation · Model 68091-38 · UDI-DI 00843696130985
1
510(k) clearances
5
Adverse events
13
Recalls
80
Facilities
Description
Front Closing Special Procedure Apron 0.5 mm front protection, 0.25 mm back protection, 21" x 36", Small, Shimmering 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.