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Henry Schein

HENRY SCHEIN, INC. · Model 5701389 · UDI-DI 00304040108321

IWO

510(k) clearances

Adverse events

Recalls

Facilities

Description

Maxi-Gard X-Ray Lead Apron

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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Data 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.