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Consumer Recalls Daily2026-07-12July 12, 2026

Consumer Recalls Daily — 2026-07-12

TITLE: Recall Digest: Death-Risk Gun Safes, Bed Rails & Baby Loungers Lead Surge in CPSC Actions; Amgen, CareFusion Face Multiple FDA Class II Recalls

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CPSC: Consumer Product Recalls

Death & Serious Injury Risk — Lead Items

  • BBRKIN's biometric gun safes (Amazon-exclusive, item 26607) can be opened by unauthorized users due to a faulty biometric lock, posing a serious injury hazard and risk of death; consumers should immediately disable the biometric feature.
  • Moodooy bed rails sold on Amazon by Yuezhang (26608) violate the mandatory adult portable bed rail standard, creating entrapment and asphyxiation hazards with a risk of death between the rail and mattress.
  • Vevor baby loungers (26591) violate infant sleep product standards — sides too low and foot openings too wide — creating fall and entrapment hazards with risk of death to infants.
  • WonderStone infant walkers sold on Walmart.com (26609) violate the mandatory infant walker standard, fitting through doorways and failing to stop at stair edges, risking serious injury or death from falls.
  • AMASKY nursing pillows sold on Amazon by Pretty-Life (26596) violate mandatory infant support cushion standards and can obstruct infant breathing, posing a suffocation death risk.
  • Topyond pool drain covers sold by Jialyduu (26592) violate the Virginia Graeme Baker Pool & Spa Safety Act, creating deadly entrapment and drowning hazards for pool users.
  • Flaunt MagSafe battery chargers (26610) contain lithium-ion cells that can overheat and ignite, posing fire and burn hazards with risk of serious injury or death.
  • Treatlife Technology's Amazon-exclusive smoke/CO combination detectors (26582) can fail to alert users to fire, risking death or serious injury from smoke inhalation or burns.

Button-Battery & Magnet Ingestion Cluster

A wave of children's products this cycle share the same lethal defect — accessible button-cell or coin batteries and high-powered magnets: Junpower CR2032 batteries sold on Amazon (26600) lack Reese's Law-required child-resistant packaging; POPOOO's LED finger light toys (26594), Honlyne's LED party favors (26580), and Raychy's children's light sneakers (26578) all violate mandatory button-cell/toy standards; Small Fish's Montessori busy boards (26579) violate toy standards via detachable high-powered magnets. All pose ingestion risks that can cause serious internal injury or death in children.

Fire & Burn Hazards

Best Buy's Insignia gas ranges (26606) have front knobs that can be accidentally activated by people or pets, risking fire injury. Greenworks' 24V/48V Kobalt yard tools with USB-C batteries (26611) can short-circuit when charged while inserted in the tool. Rowenta cordless vacuums (26595) contain lithium-ion batteries prone to overheating and ignition. Daikin/Amana air conditioners and heat pumps (26581) can stay energized during a ground fault despite being switched off. Cooper Lighting's Metalux High Bay LED fixtures (26599) can overheat and ignite nearby combustibles.

Other Notable Recalls

Conair's Cuisinart Propel+ gas grills (26605) have pizza-oven glass windows prone to shattering, and separately Conair recalled over one million Cuisinart grill brushes (26601) whose wire bristles can detach and cause internal injury requiring surgery. Diamond Wipes International's CVS Health medicated hemorrhoidal wipes (26593) lack required child-resistant packaging despite containing lidocaine, risking child poisoning. Kith Retail's children's loungewear sets (26507) violate flammability standards for sleepwear. Winco Fireworks International recalled two products — Roman Candles 8-Shot (26603) and Unity 7-Shot 200-gram Aerial Cakes (26602) — both prone to malfunction, tipping, or blowouts causing explosion/burn injuries. Target's Gigglescape Under the Sea popping toy (26598) has a dome that detaches, exposing small balls as a choking hazard.

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FDA: Drug & Device Recalls (All Class II)

Amgen Inc. issued three separate Class II recalls this cycle for foreign-substance or manufacturing defects: Corlanor (ivabradine) 7.5mg tablets (D-0615-2026, NDC 55513-810-60) and 5mg tablets (D-0612-2026, NDC 55513-800-99/60) both cite presence of a foreign substance; Sensipar (cinacalcet) 60mg tablets (D-0614-2026, NDC 55513-074-30) were pulled for CGMP deviations.

CareFusion 213, LLC (a Becton, Dickinson subsidiary) recalled two BD ChloraPrep antiseptic applicator lines — BD ChloraPrep Clear 1mL applicators (D-0622-2026) and BD ChloraPrep FREPP Clear 1.5mL applicators (D-0623-2026) — both for wrinkled paper lidding that may breach sterility seals.

Other single-product actions: Annora Pharma/Camber Pharmaceuticals' Lacosamide 100mg tablets (D-0626-2026, NDC 31722-813-60) were recalled after a complaint of a Selexipag tablet mix-up in the bottle. Ajanta Pharma USA's Fenofibrate 200mg capsules (D-0611-2026, NDC 27241-120-04) cite CGMP deviations. Direct Rx's Duloxetine D/R capsules (D-0617-2026, NDC 61919-482-30/60, marketed as Cymbalta) were recalled for elevated N-nitroso-duloxetine impurity above FDA's interim limit. Elevate Oral Care's Povi-One 10% povidone-iodine oral antiseptic (D-0627-2026, NDC 57511-0611-1) was recalled for sub-potency. Central Admixture Pharmacy Services recalled a patient-specific pediatric TPN compound bag (D-0618-2026) after it was found missing copper and famotidine per label.