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Bartels

CLARK LABORATORIES, INC. · Model B1029-37 · UDI-DI 05391516747271

KIT
1
510(k) clearances
5
Adverse events
4
Recalls
25
Facilities

Description

Tissue Culture Refeeding Medium

Recalls

DateFirmReason
2018-08-24Life Technologies, Corp.Leaky bottles due to a defect in the bottle cap compromising the sterility of the product
2018-08-24Life Technologies, Corp.Leaky bottles due to a defect in the bottle cap compromising the sterility of the product
2018-08-24Life Technologies, Corp.Leaky bottles due to a defect in the bottle cap compromising the sterility of the product
2018-08-24Life Technologies, Corp.Leaky bottles due to a defect in the bottle cap compromising the sterility of the product

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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.