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Quintest® Covered Tray

Jubilant Hollisterstier LLC · Model 8930ZA · UDI-DI 00365044000073

LDH Prescription
1
510(k) clearances
3
Adverse events
3
Recalls
6
Facilities

Description

60 hole covered test tray

Recalls

DateFirmReason
2016-03-22Medscience IncDuring an FDA inspection it was found that the products are marketed without a cleared 510k.
2015-02-03Allergy Laboratories, Inc.Potential for glass particles within the vials
2006-04-20Hollister Stier Laboratories LLCPotential for vials to be cracked at the vial stopper interface. This could compromise the sterility of the products compounded into the vials.

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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.