FDAAugust 13, 2018device

remel THIOGLYCOLLATE MEDIUM W/O IND. W/ DEXTROSE W/ HEMIN & VIT.K (a) 10ML, REF 07182 (b) 10ML, REF 07180 (c) 5ML, REF 064732 (d) 5ML, REF 064730 (e) 9ML, REF 064720

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Products have intermittently failed performance testing during stability studies with various anaerobic microorganisms.

What to do

FDA enforcement status: Terminated

Brands named

remel

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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