
FDA•MODERATE
FDR Visionary Suite X-ray Generator
FUJIFILM is recalling FDR Visionary Suite X-ray generators due to a risk of overheating and smoke caused by faulty electromagnetic contactors.

FUJIFILM is recalling FDR Visionary Suite X-ray generators due to a risk of overheating and smoke caused by faulty electromagnetic contactors.

Biomerieux is recalling 30+ VITEK 2 susceptibility cards due to potential quality control failures and false resistant test results.
2 products
Vantive is recalling the Prismaflex M100 Set due to a potential dislodgement of the deaeration chamber from the control unit.
8 products
Unichem Pharmaceuticals recalls Bisoprolol/Hydrochlorothiazide 2.5/6.25 mg tablets (NDC 29300-187-01) due to N-Nitroso Bisoprolol impurity specification failure.

Why Not Natural is recalling Moringa Capsules distributed nationwide due to potential Salmonella contamination.

Greenstone is recalling methylprednisolone 4 mg tablets (NDC 59762-4440-2) due to incorrect blister foil orientation causing incorrect dosing information.

Rising Pharmaceuticals is recalling Furosemide Tablets 40 mg (NDC 64980-563-10) due to foreign substance contamination.

Specialty Process Labs is recalling Thyroid, USP (NDC 81305-100-02) due to subpotency.

Live it Up Super Greens recalled over possible Salmonella Typhimurium contamination.
4 products
Cipla is recalling Lanreotide Injection 120 mg/0.5 mL due to the presence of particulate matter.

Encon Safety Products is recalling AQ 120 GFEW Aquarion Preserved Cartridges due to cGMP manufacturing deviations.

Spring & Mulberry recalls 11 varieties of Date-Sweetened Chocolate bars over potential Salmonella contamination.
11 products
Diva Fam recalls all flavors of Sea Moss Gel Superfood (16 oz) over botulism risk.
14 products
HerbsForever recalls Gastro Care and Hingwastika Churna supplements over undeclared wheat allergen.
2 products