Remel Inc recalls remel THIOGLYCOLLATE MEDIUM W/O INDICATOR. W/ DEXTROSE (a) 9ML, REF 064700 (b) 10ML, REF 07176 (c) 9ML, REF 064702

Recalled September 19, 2018 · FDA recall Z-3018-2018 · Remel

Hazard

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

Units

384 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 INDICATOR. W/ DEXTROSE (a) 9ML, REF 064700 (b) 10ML, REF 07176 (c) 9ML, REF 064702

Manufacturer(s)

Remel Inc

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