Consumer Recalls Daily — 2026-06-06

TITLE: Consumer Recalls Daily — June 6, 2026: Death-risk helmets, pool drain covers, and a Class I skincare contamination

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CPSC — Consumer Products

Lead: Death-or-serious-injury hazards

• [26528] Bicycle helmets sold on Amazon by Gudook Outdoor Sports were recalled June 4 after failing the mandatory CPSC impact-attenuation and certification requirements, leaving riders unprotected in a crash and posing a risk of serious head injury or death.
• [26527] and [26529] Two separate Amazon sellers — Eicong (Crenlux-branded) and Broqixin — recalled pool drain covers that violate the Virginia Graeme Baker Pool & Spa Safety Act's entrapment-protection standards, creating deadly entrapment and drowning hazards for swimmers and bathers.
• [26525] Little Grape Land nursing pillows were recalled for violating the mandatory standards for nursing pillows and infant support cushions; the products can obstruct an infant's breathing and pose a suffocation death risk.
• [26531] SUNS International recalled residential elevator interlock switches after finding the switches can stick in a retracted position, leaving the exterior door unlocked and creating a fall/crushing death risk if the elevator is called to another floor.
• [26522] Walmart recalled its Mainstays 9-Drawer Fabric Dressers (made by Hop Thang Interior Wood Co., Vietnam) for violating the mandatory clothing-storage-unit standard; the unanchored units are unstable and pose tip-over and entrapment death risks to children.
• [26501] Lil Pick Up recalled youth ATVs that violate the federal ATV standard — mechanical suspension fails and the reverse indicator light does not illuminate — creating crash and burn hazards with a risk of serious injury or death.
• [26502] PandaEar portable hook-on chairs were recalled because the crotch restraints can be removed without a tool, allowing infants to fall through an opening in violation of the mandatory hook-on chair standard.
• [26504] Bethlehem Lights 10-inch Illuminated Ribbon Spheres sold by QVC were recalled after LED components were found to overheat, posing a serious fire and death risk.

Battery, magnet, and toxic-substance hazards in children's products

A cluster of recalls this cycle targets children's products that breach the mandatory toy standard or Reese's Law:

• [26510] Lithium coin batteries imported by Proudly American Store (Canada) lack child-resistant packaging and Reese's Law warning labels, posing internal chemical-burn and death risk if swallowed.
• [26515] Luminous Fidget Spinner Balls sold on Amazon by Anzmtosn (Shenzhen Bangduola Electronic Technology) and [26514] Missry Associates' Misco Sports Light-Up Racket Sets were recalled because button cell batteries are easily accessible to children.
• [26497] and [26503] ABC Trading recalled two product lines — unnamed children's toys and WSDZ Light-up Glasses — for the same button-cell accessibility violations.
• [26509] Daoen Zen Magnetic Promotional Ball Sets and [26508] MiniWarGaming/Primal Horizon Disc Magnets were recalled as loose high-powered magnets exceeding CPSC flux limits, posing deadly ingestion hazards.
• [26499] The Orb Factory recalled Orb Funkee squeeze toys after fibrous tremolite asbestos was identified in the sand filler, with health risks from inhalation.

Fire, burn, and mechanical hazards

• [26524] Wyze Labs recalled its Solar Cam Pan security cameras because incorrect assembly instructions can cause consumers to puncture the lithium-ion battery casing, leading to rapid overheating, fire, and burn injuries.
• [26532] Vornado Air SRTH Small Room Tower Heaters were recalled after the fan blade can detach from the motor shaft, causing internal parts to melt and potentially ignite — breaching the enclosure.
• [26513] Zhejiang Mingrui Furniture (Joy Furniture) recalled its Talan and Royce living room sets because the power switch on the sofa, loveseat, or recliner can malfunction and overheat, posing a fire-related serious injury risk.
• [26511] Tzumi Electronics SLF Sauna Blankets and [26506] Giantex/Costway Portable Steam Saunas were recalled for overheating and steam-burn hazards, respectively.
• [26512] Giantex also recalled lounge chairs with a pinch point at the recline adjuster that poses an amputation hazard.
• [26530] TOMY recalled Boon NURSH 8 oz reusable baby bottles sold at Walmart because the hard plastic outer shell can bubble and peel, shedding film-like fragments that pose a choking hazard.
• [26526] Tiny Land recalled children's play tents whose fiberglass poles can shed fibers, causing skin and eye irritation.

FDA — Drugs and Biologics

Class I lead

• [D-0553-2026] Wisconsin Pharmacal Company initiated a Class I recall on April 24 of MG217 Multi-Symptom Treatment Cream & Skin Protectant (colloidal oatmeal 2%, 6 oz; manufactured at Pharmacal, Jackson, WI) after confirming *Staphylococcus aureus* contamination of the non-sterile product — the only Class I event in this cycle.

Class II — sterility, potency, and labeling failures

• [D-0546-2026] UCB Biosciences recalled Cimzia (certolizumab pegol) 2x200 mg/mL prefilled syringes (NDC 50474-710-79/-80/-81), including starter kits and professional samples, for lack of assurance of sterility — a notable hit on a widely used biologic.
• [D-0548-2026] IntegraDose Compounding Services (Shoreview, MN) recalled compounded fentanyl citrate sterile CADD injection 2,500 mcg/50 mL (NDC 71139-6030-1) as subpotent, raising under-dosing concerns for pain-pump patients.
• [D-0541-2026] Lupin Pharmaceuticals recalled liraglutide injection 18 mg/3 mL pens (NDC 70748-346-02 and -03), manufactured in Nagpur, India, after a white thread-like particulate was identified in the cartridge.
• [D-0545-2026] and [D-0544-2026] Zydus Pharmaceuticals (USA) recalled both erythromycin tablets 250 mg (NDC 70710-1047-3) and 500 mg (NDC 70710-1048-3), manufactured by Zydus Lifesciences in Ahmedabad, for CGMP deviations and N-Nitroso-Desmethyl-Erythromycin levels above the recommended intake limit — an expanding nitrosamine-impurity story.
• [D-0538-2026] Safecor Health (Columbus, OH) recalled unit-dose atomoxetine HCl capsules (NDC 64380-474-01) after 25 mg capsules were incorrectly labeled as 10 mg — a 2.5× overdose risk for ADHD patients.

Class III — primidone cross-contamination

A coordinated Class III primidone recall hit three repackagers/marketers, all citing API cross-contamination with trace Acemetacin:

• [D-0537-2026] Amerisource Health Services / American Health Packaging primidone 50 mg unit-dose cartons (NDC 68084-202-01/-11).
• [D-0534-2026] and [D-0535-2026] Golden State Medical Supply primidone 50 mg (NDC 51407-637-05) and 250 mg (NDC 51407-638-01) bottles, manufactured by Lannett.

The shared Lannett-API root cause suggests epilepsy patients on primidone should check bottle NDCs against pharmacy records.