Home › Flow X Ray Corporation › Apronette, Standard Lead, 18" x 24"
Apronette, Standard Lead, 18" x 24"
Flow X Ray Corporation · Model 69098-16 · UDI-DI 00843696129019
1
510(k) clearances
5
Adverse events
13
Recalls
80
Facilities
Description
Apronette, Standard Lead, 18" x 24", Medium Blue
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.