Remel Inc recalls Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R0150
See all recalls from Remel Inc →Recalled Product
Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm plates REF R04033,
Hazard / Issue
Test organisms exhibit poor growth when grown using the test agar. The poor growth can give users incorrect AST zones when performing susceptibility tests.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: A) Lot: 978596, 2017-01-30; B) Lot: 978948, 2017/01/30
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
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