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Remel Inc recalls remel THIOGLYCOLLATE MEDIUM, REF 05152
Recalled September 19, 2018 · FDA recall Z-3019-2018 · Remel
Hazard
Products have intermittently failed performance testing during stability studies with various anaerobic microorganisms. · FDA Class II
Units
48 units
Sold at
US, Canada, Singapore
Description
Products have intermittently failed performance testing during stability studies with various anaerobic microorganisms.
Product
remel THIOGLYCOLLATE MEDIUM, REF 05152
Manufacturer(s)
Remel Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →