Medical device recalls Moderate risk

Remel Inc recalls remel THIOGLYCOLLATE MEDIUM, REF 05152

Recall date
August 13, 2018
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-3019-2018
FDA classification
Class II
Brand / firm
Remel Inc
Sold / distributed
US, Canada, Singapore

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

remel THIOGLYCOLLATE MEDIUM, REF 05152

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