Severity 2 of 5
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Severity 2 (Moderate) recalls cover minor labeling errors, low-risk contamination, and voluntary precautionary recalls. The agency's own classification is typically FDA Class III, or the issue is something like incomplete instructions or a small UPC mismatch where the product itself is safe but doesn't meet documentation requirements. Use the same brand-name product safely; follow the manufacturer's instructions for return or exchange if you want a refund.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Iowa Select Herbs LLC is recalling Valerian Root under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Fenugreek Seed because it is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Cinnamon Bark products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Burdock Root under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Fujifilm Medical Systems is recalling 2,062 Smart CR Digital Computed Radiography Systems due to reports of power supply failure.
Iowa Select Herbs LLC is recalling Ginger Root products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Medtronic is recalling CareLink and CareLink Express monitors because a firmware update contained incorrect dial-up configuration data, potentially preventing data transmission to the CareLink Network.
Iowa Select Herbs LLC is recalling 10 bottles of 4 fl. oz. Aloe Vera Juice because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Mako Surgical Corporation is recalling 10 units of the MAKOplasty Hip Array Kit Laminate 150230 because the product may list two part numbers for the RIO Base Array.
Iowa Select Herbs LLC is recalling Schizandra Berry under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
VistaPharm is recalling 8,901 cases of Oxycodone Hydrochloride Oral Solution because defective container seals may allow the medication to leak.
Iowa Select Herbs LLC is recalling Astragalus Root products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Lemon Balm Leaf products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling 24 bottles of Yarrow Flowers because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling 1-gallon bottles of Magnolia Bark because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Ziziphus supplements because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Eleuthero Root under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Red Ginseng Root under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling 1-gallon bottles of Alcohol-Free Raspberry Leaf because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling 10 bottles of Arnica Flowers because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Quack Grass dietary supplements because they are misbranded, unapproved new drugs, and adulterated.
Iowa Select Herbs LLC is recalling Oatstraw products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling 1-gallon bottles of Alcohol-Free Chicory Root because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Bilberry Leaf products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Radiometer America is recalling TCM CombiM Modules 903-111 because the alarm may sound louder than the pre-set maximum volume.