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Henry Schein

HENRY SCHEIN, INC. · Model 1003048 · UDI-DI 00304040059623

KSD
1
510(k) clearances
10
Adverse events (1 deaths)
1
Recalls
18
Facilities

Description

Impulse Heat Sealer

Recalls

DateFirmReason
2011-01-31Haemonetics CorporationBattery pack may have exposed wire becoming hot

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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.