FDAFebruary 9, 2017device
Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm plates REF R04033,
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Test organisms exhibit poor growth when grown using the test agar. The poor growth can give users incorrect AST zones when performing susceptibility tests.
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.
- FDAOxoid Agglutinating Sera, Salmonella 9-0 R309573012026-03-25
- FDAYeastone Broth, 11ML, 10/BOX YY34622026-03-24
- FDACampy CVA Medium 100/PK, R012722026-02-05
- FDA1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT34502025-11-12
- FDABlood Agar,5% Sheep Blood 100/PK, Product Number R012022025-07-11
- FDAStrep Selective II Agar, Product Number R018592025-07-11
- FDABlood/MacConkey Biplate 100/PK, Product Number R020492025-07-11
- FDABlood/EMB, Levine 100/PK, Product Number R020412025-07-11
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