Remel Inc recalls remel THIOGLYCOLLATE MEDIUM W/O IND. W/ DEXTROSE W/ HEMIN & VIT.K (a) 10ML, REF 07182 (b) 10ML, REF 07180 (c) 5ML, RE

Recalled September 19, 2018 · FDA recall Z-3017-2018 · Remel

Hazard

Products have intermittently failed performance testing during stability studies with various anaerobic microorganisms. · FDA Class II

Units

2730 units

Sold at

US, Canada, Singapore

Description

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

Product

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

Manufacturer(s)

Remel Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →