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.
Cefla Dental Group is recalling 173 MyRay RXDC dental x-ray units because they lack required certification and identification labels.
Clement Pappas & Co. is recalling Giant Eagle Nature's Basket Organic Apple Juice because it contains patulin levels between 57.4 and 100 ppb.
Boston Scientific is recalling the LATITUDE Patient Management System software because a system update caused clinic faxes to display illegible characters instead of required patient information.
Lloyd Inc. of Iowa is recalling bulk Thyro-Tab tablets due to cGMP deviations and stability failures. The product was repackaged by Forest Laboratories and distributed nationwide.
Lloyd Inc. of Iowa is recalling Levothroid (levothyroxine sodium) tablets due to cGMP deviations and insufficient stability data.
King Legacy is recalling Levoxyl tablets that were below specification for potency at the expiry stability point.
Lloyd Inc. of Iowa is recalling Levothroid tablets due to cGMP deviations and stability failures in previous lots.
Coloplast is recalling 111 units of Restorelle L prostheses because the packaging contains incorrect Instructions For Use pamphlets.
Lloyd Inc. of Iowa is recalling 7.6 million Thyro-Tab tablets due to cGMP deviations and stability failures. The product was distributed nationwide and to Puerto Rico.
Progressive Medical is recalling PTFE coated disposable electrosurgical electrodes because product coatings require 510K approval.
Lloyd Inc. of Iowa is recalling bulk Thyro-Tab 0.088 mg tablets due to cGMP deviations and stability failures. The product was repackaged by Forest Laboratories and distributed nationwide.
Philips is recalling 515 CT systems because they stored the sum of CTDIVol values instead of individual slice values, resulting in incorrect data.
Clement Pappas & Co. is recalling Wild Harvest Organic Apple Juice because it contains patulin levels between 57.4 and 100 ppb.
Progressive Medical is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Lloyd Inc. of Iowa is recalling 9.5 million Thyro-Tab tablets due to cGMP deviations and insufficient stability data.
Lloyd Inc. of Iowa is recalling Levothroid (levothyroxine sodium) tablets due to cGMP deviations and insufficient stability data.
Lloyd Inc. of Iowa is recalling Levothroid tablets due to cGMP deviations and insufficient stability data. The recall affects 12,156 bottles distributed nationwide and to Puerto Rico.
King Legacy is recalling Levoxyl tablets because they were below specification for potency at the expiry stability point.
Clement Pappas & Co. is recalling Giant Eagle Nature's Basket Organic Cranberry Juice because an ingredient contained patulin levels between 57.4 and 100 ppb.
ConMed Linvatec is recalling 267 VP1600 HD Still Capture Systems due to a software anomaly that may cause the device to lock up.
King Legacy is recalling Levoxyl (levothyroxine sodium) tablets because they were below specification for potency at the expiry stability point.
Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Clement Pappas & Co. is recalling Publix Greenwise Organic Cranberry Flavored Juice Blend because an ingredient contained patulin levels between 57.4 and 100 ppb.
Clement Pappas & Co. is recalling Organic Nature's Promise Organic Cranberry Juice Blend because an ingredient contained patulin levels above the limit.
Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.