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Fisherbrand

FISHER SCIENTIFIC COMPANY L.L.C. · Model 02 544 208 · UDI-DI 00613647005958

KDT Prescription

510(k) clearances

287

Adverse events

Recalls

113

Facilities

Description

SPECIMEN COLLECTION SYST 60/CS

Recalls

Date	Firm	Reason
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads

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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.