Consumer Recalls Daily — 2026-06-02

TITLE: Recalls Daily — Magnet & button-cell toys dominate CPSC docket; Class I skin cream pulled by FDA

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CPSC — Consumer Products

Lead: Child ingestion and tip-over hazards

The May 2026 CPSC docket is dominated by repeat-offender hazard classes — high-powered magnets, accessible button-cell batteries, and unanchored furniture — nearly all flagged with risk of "serious injury or death."

• 26509 (Daoen Zen Magnetic Promotional Ball Sets) and 26508 (MiniWarGaming/Primal Horizon disc magnets) were both pulled May 28 for violating the mandatory magnet standard; the loose high-powered magnets fit within CPSC's small-parts cylinder and can attract through bowel tissue if multiples are swallowed.
• A cluster of button-cell battery toys was recalled the same week: 26515 (Anzmtosn Luminous Fidget Spinner Balls, sold on Amazon by Shenzhen Bangduola), 26514 and 26483 (Missry Associates' Misco Sports light-up racket and badminton sets), 26503 and 26497 (ABC Trading's WSDZ light-up glasses and assorted children's toys) — all citing accessible compartments and risk of esophageal burns from swallowed coin cells.
• 26510 (Proudly American Store, Canada) and 26484 (LiCB / Guangzhou Lichengbei, sold on Amazon) recall loose lithium coin batteries shipped without Reese's Law-compliant child-resistant packaging or warning labels.
• 26522 — Walmart recalled Mainstays 9-Drawer Fabric Dressers (made by Vietnam's Hop Thang Interior Wood) for failing the mandatory clothing storage unit stability standard; unanchored units pose tip-over and entrapment death risks to children.
• 26502 (PandaEar portable hook-on chairs) violates the hook-on chair standard because crotch restraints detach without tools, allowing infants to fall through; 26493 (Cosyland children's tower stools) and 26490 (Guidecraft standing towers) round out a bad week for kitchen-helper towers, citing collapse, tip-over, and torso entrapment.

Fire, burn, and carbon-monoxide hazards

• 26494 — Generac Power Systems (Waukesha, WI) expanded its recall of Generac and DR Power electric-start pressure washers; a malfunctioning start/stop button can self-start the engine, posing a fatal CO poisoning risk in enclosed spaces. Additional models have been added to the prior action.
• 26513 (Joy Furniture / Zhejiang Mingrui's Talan and Royce illuminated living-room sets) and 26504 (Bethlehem Lights LLC's 10-inch Illuminated Ribbon Spheres, sold via QVC) were both recalled for LED assemblies that can overheat and ignite.
• 26511 (Tzumi Electronics SLF Sauna Blankets) and 26506 (Giantex/Costway portable steam saunas) carry burn and fire hazards from overheating elements and misaligned steam diffusers, respectively.

Vehicles and mechanical injury

• 26482 — BRP recalled Can-Am ATVs after finding the speed-limiter control can malfunction and cause unexpected acceleration; consumers are told to stop using Speed Limiter Mode pending repair.
• 26501 — Lil Pick Up youth ATVs fail the federal ATV safety standard on suspension and reverse-indicator lighting, posing crash and burn risks.
• 26479 (Minka Lighting Bardon Series pendants) can detach from the downrod during installation; 26486 (Amazon Basics 55 lb. Adjustable Dumbbells), 26498 (HomeProGym resistance bands), and 26512 (Giantex lounge chairs) all involve impact or amputation hazards from components that separate or pinch under load.

Notable chemical hazard

• 26499 — The Orb Factory's Orb Funkee squeeze toys were recalled after fibrous tremolite asbestos was identified in the sand fill; consumers are told to remove the toys from children immediately. Asbestos contamination in a children's tactile toy is a rare and serious finding.

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FDA — Drugs

Lead: Class I — bacterial contamination in OTC skin cream

• D-0553-2026 — Wisconsin Pharmacal Company (Jackson, WI) is recalling MG217 Multi-Symptom Treatment Cream & Skin Protectant (colloidal oatmeal 2%, 6 oz tubs) at Class I after confirmed *Staphylococcus aureus* contamination of the non-sterile cream — a serious risk for users with broken skin or eczema, the product's core demographic.

Class II — sterility, potency, and nitrosamine impurities

• D-0546-2026 — UCB Biosciences recalled Cimzia (certolizumab pegol) 2×200 mg/mL prefilled syringes (NDC 50474-710-79/-80/-81, including starter kits and professional samples) for lack of sterility assurance.
• D-0548-2026 — IntegraDose Compounding Services (Shoreview, MN) pulled compounded fentanyl citrate sterile CADD bags, 2,500 mcg/50 mL (NDC 71139-6030-1), as subpotent — a notable concern for pump-dependent pain patients.
• D-0544-2026 and D-0545-2026 — Zydus Pharmaceuticals (USA) recalled erythromycin tablets at both the 250 mg (NDC 70710-1047-3) and 500 mg (NDC 70710-1048-3) strengths, manufactured by Zydus Lifesciences in Ahmedabad, for cGMP deviations producing N-Nitroso-Desmethyl-Erythromycin above the recommended intake limit.
• D-0541-2026 — Lupin Pharmaceuticals recalled liraglutide injection 18 mg/3 mL pens (NDC 70748-346-02 and -03), made at Lupin Limited's Nagpur site, after a white thread-like particulate was found in cartridges.
• D-0538-2026 — Safecor Health (Columbus, OH) recalled unit-dose atomoxetine HCl 10 mg capsules (NDC 64380-474-01) after a label mix-up: 25 mg capsules were packed into 10 mg-labeled foil strips — a 2.5× overdose risk for pediatric ADHD patients.

Class III — primidone cross-contamination cluster

Three separate primidone recalls trace to Lannett Company API contaminated with trace acemetacin (an NSAID):

• D-0537-2026 — American Health Packaging primidone 50 mg unit-dose cartons (NDC 68084-202-01 / -11), repackaged by Amerisource Health Services.
• 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 and marketed by GSMS (Camarillo, CA).

The shared root cause suggests pharmacists and epilepsy clinics should check inventory against the Lannett API lots feeding all three labelers.