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TITANIUM VAC REG

HERSILL SL · Model CONT/INT OM*INT TRAP · UDI-DI 08435510679774

KDP Prescription
10
510(k) clearances
99
Adverse events (6 deaths)
4
Recalls
29
Facilities

Description

VACUSILL 3 REG CONTINUOUS INTERMITTENT + OM WALL CONNECTION + SAFETY TRAP

Recalls

DateFirmReason
2018-03-12Ohio Medical CorporationFinal quality control testing was not completed before the devices were distributed..
2005-08-01Boehringer Laboratories, Inc.Condition exists that prevents complete shutoff of the valve
2005-08-01Boehringer Laboratories, Inc.Condition exists that prevents complete shutoff of the valve
2005-08-01Boehringer Laboratories, Inc.Condition exists that prevents complete shutoff of the valve

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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.