Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Fresenius Kabi is emphasizing instructions for large volume parenteral (LVP) programming duration in the Ivenix Infusion System software. 30 units were distributed nationwide.
PALACOS R+G pro bone cement is recalled due to defects that prevent ampoule breakage, blocking cement dough formation and making the product unusable.
Gold Star Distribution Inc. is recalling all lots of Pepto Bismol 32-count tablets distributed nationwide due to Current Good Manufacturing Practice deviations—insanitary conditions and rodent activity identified at their distribution center.
Gold Star Distribution Inc recalls all lots of Liquid NyQuil (regular and cherry, 12/8oz bottles) distributed nationwide due to insanitary conditions and rodent exposure at their distribution facility.
Medline has recalled Neuro Angio Packs containing B. Braun IV and pump administration sets because check valve components may become stuck in open or closed positions, potentially affecting medication delivery.
In limited Allura Xper FD20 X-ray systems, the cooling unit drip tray was not installed or inadequately documented. This creates a potential for coolant to contact electrical components and trigger system shutdown.
Heraeus Medical is recalling PALACOS MV+G pro bone cement due to ampoules that may fail to break properly, preventing product use. Affected units were distributed internationally.
Philips is recalling select Allura Xper FD20/20 imaging systems where the cooling unit drip tray may not be installed. If not installed, coolant could contact electrical components and cause system shutdown.
BD Ready-to-Use Hydrophilic Catheters (14 Fr, Straight Tip, Female) are being recalled due to incorrect expiration date labeling. The recall affects 149,310 units distributed in Georgia.
Philips is recalling 38 Allura Xper FD10C medical imaging systems in which the cooling unit drip tray may not be properly installed, potentially allowing coolant to contact electrical components and cause system shutdown.
Encon Safety Products is recalling its AQ 120 GFEW Aquarion Preserved Cartridges nationwide due to current Good Manufacturing Practice deviations. The voluntary recall affects 7,677 bags distributed across the United States.
SUN Pharmaceutical recalls Clindamycin Phosphate 1% topical solution nationwide due to failed quality control tests showing out-of-specification impurities and assay results. Affected lots should be discontinued.
Sun Pharmaceutical is recalling Fluocinolone Acetonide Solution topical solution distributed nationwide due to manufacturing quality issues. Testing found an impurity level that exceeded specifications.
Curtis International is recalling about 330,000 Frigidaire model EFMIS121 minifridges because internal electrical components can short circuit and cause fires. At least six incidents with property damage have been reported.
Greatale self-feeding pillows hold bottles at an unsafe angle and prevent infants from pulling away, creating a risk of aspiration and suffocation. About 1,260 units sold online have been recalled.
Ruahouine Hair Growth Serum bottles containing minoxidil lack legally-required child-resistant packaging. About 25,000 units sold on Amazon present a serious risk of poisoning if ingested by young children.
Energizer is recalling about 4,100 Large Power Indicator Lanterns with June 2024 date codes due to lithium-ion batteries that can overheat, posing a burn hazard. No injuries have been reported.
R.X.Y bicycle helmets sold online have been recalled because they violate safety standards and may fail to protect riders in a crash. No injuries have been reported.
BBWOO Baby Loungers are recalled due to entrapment and fall hazards that violate infant sleep safety standards. The sides are too low, foot openings are too wide, and the product lacks a stand.
RootStim Beard Growth Serum bottles are not in child-resistant packaging as required by the Poison Prevention Packaging Act. The minoxidil contents pose a risk of serious injury or death if swallowed by young children, though no injuries have been reported.
Yixing Trading is recalling about 1,500 KEAWIS crib mattresses due to entrapment and suffocation hazards. The mattresses may not fit certain play yards or cribs properly, creating gaps where infants could become trapped.
Adams Manufacturing and StyleWell recall about 6,100 Adirondack patio chairs that can crack and collapse, posing fall and injury hazards. No injuries have been reported. Consumers should stop using the chairs and return them for a full refund.
Morgan Lane is recalling about 95 Asher Pajama Sets sold from March 2024 through May 2025 due to flammability hazard. The pajamas violate mandatory safety standards for children's sleepwear and pose a burn risk.
HEZI brand power strips with ungrounded metal enclosures pose electrocution hazard. About 1,320 units sold online from May 2024 through October 2025. Consumers should stop using and request full refund from HEZI HOME.
GBC Food Services is recalling EverRoast Chicken Caesar Wraps (11.25 oz, UPC 85004224455) distributed in Kentucky and Indiana due to the potential presence of Listeria monocytogenes. Affected products have best-by dates from November 9, 2025 to November 22, 2025.