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FDA Warning Letter to Supercan Bully Sticks LLC

The FDA issued a warning letter to Supercan Bully Sticks LLC on September 24, 2025, following inspections that revealed serious violations of the Foreign Supplier Verification Program (FSVP) and Current Good Manufacturing Practice regulations. These violations were identified after a voluntary recall of pet treats due to Salmonella contamination.

HHS OIG: Colorado Medicaid Improper Payments for ABA Services

The HHS Office of Inspector General (OIG) found that Colorado made at least $77.8 million in improper fee-for-service Medicaid payments for Applied Behavior Analysis (ABA) services provided to children in 2022 and 2023. The OIG recommended Colorado refund $42.6 million to the Federal Government and improve guidance for ABA providers.

FDA Import Alert: GLP-1 Receptor Agonist Bulk Drug Substances

The FDA has issued Import Alert #66-80, placing Glucagon-Like Peptide-1 (GLP-1) Receptor Agonist Bulk Drug Substances on Detention Without Physical Examination. This action is due to concerns that these substances, used in compounding, may be adulterated and not meet current good manufacturing practice (CGMP) requirements.

FDA Import Alert 16-120: Detention of Non-Compliant Fish Products

The FDA has updated Import Alert 16-120, revising guidance for field personnel regarding the detention without physical examination (DWPE) of fish and fishery products from foreign processors not in compliance with the Seafood HACCP regulation. The update includes changes to the title, reason for alert, and guidance sections, incorporating foreign remote regulatory assessments as a compliance verification method.

FDA Import Alert 98-06: New Tobacco Products Detained Without Authorization

The FDA has updated Import Alert 98-06, which detains new tobacco products lacking required marketing authorization. This revision clarifies guidance and agency contacts, noting that ENDS products are now covered under a separate alert (98-07). Manufacturers and importers must ensure proper authorization to avoid detention.

Trankerloop Baby Bath Seats Recalled Due to Drowning Risk

The U.S. Consumer Product Safety Commission (CPSC) announced the recall of approximately 2,380 Trankerloop baby bath seats due to a drowning risk. The seats violate mandatory safety standards for infant bath seats because they are unstable and can tip over. Consumers are advised to stop using the product and contact Trankerloop for a full refund.

Sanven Technology Recalls Vevor Baby Gates for Injury Risk

Sanven Technology is recalling Vevor baby gates due to an entrapment hazard that violates mandatory safety standards and poses a risk of serious injury. Consumers are urged to stop using the recalled gates immediately and contact Sanven Technology for a full refund.

PQL Recalls LED Light Fixtures Due to Fire Hazard

PQL is recalling approximately 186,520 High Bay Linear LED light fixtures due to a fire hazard caused by degrading retaining pins. Consumers are advised to stop using the fixtures immediately and contact PQL for a free repair.

Weber Recalls 3.2 Million Grill Brushes Due to Ingestion Hazard

Weber is recalling over 3.2 million metal wire bristle grill brushes due to an ingestion hazard. The U.S. Consumer Product Safety Commission (CPSC) announced the recall on February 26, 2026. Consumers are advised to stop using the recalled brushes and contact Weber for a refund or replacement.

Dupray Neat Steam Cleaners Recalled Due to Burn Hazard

Dupray USA has recalled approximately 651,145 Neat Steam Cleaners due to a risk of burn hazards or serious injury from potential boiler ruptures. Consumers are advised to stop using the product immediately and obtain a free replacement safety boiler cap.