Consumer Recalls Daily — 2026-06-04

TITLE: Recalls Daily — Magnet & button-cell toys dominate CPSC sweep; Class I MG217 cream pulled for Staph contamination

CPSC — Consumer Products

Lead: Hazards citing risk of serious injury or death

• Recall 26494 expands Generac Power Systems' recall of Generac and DR Power electric-start pressure washers after the start/stop button can self-activate, posing carbon monoxide poisoning risk in confined spaces; additional models added on 2026-05-14.
• Recall 26482 covers BRP Can-Am ATVs whose speed-limiter control can malfunction and trigger unexpected acceleration, posing crash-injury and fatality risk; consumers told to stop using Speed Limiter Mode immediately.
• Recall 26501 targets Lil Pick Up youth ATVs that fail the federal ATV standard — suspensions don't meet mechanical requirements and reverse indicator lights fail — creating crash and burn hazards for child riders.
• Recall 26522 — Walmart's Mainstays 9-Drawer Fabric Dressers (made by Hop Thang Interior Wood, Vietnam) are unstable unanchored and violate the mandatory clothing storage unit standard, posing tip-over and entrapment death risks to children.
• Recall 26502 pulls PandaEar portable hook-on chairs whose crotch restraints can be removed without tools, allowing infants to fall through openings in violation of the mandatory standard.
• Recall 26493 removes Cosyland children's tower stools that can collapse or tip and whose front/back openings can entrap a child's torso.
• Recall 26490 covers Guidecraft children's standing towers whose internal platform can loosen and detach over time, dropping young users.
• Recall 26499 withdraws Orb Funkee squeeze toys imported by The Orb Factory after fibrous tremolite asbestos was found in the sand fill, an inhalation hazard for children.
• Recall 26479 removes Minka Lighting Group's Bardon Series pendant fixtures whose frame can detach from the downrod during installation, an impact hazard.

Button-cell, coin-battery, and high-powered magnet sweep

CPSC's 2026-05-21 and 2026-05-28 actions hit an unusually large cluster of toys and batteries violating the mandatory toy standard and Reese's Law on button-cell packaging — all flagged for fatal ingestion risk:

• Recall 26509 (Daoen Zen Magnetic Promotional Ball Sets) and Recall 26508 (MiniWarGaming/Primal Horizon Disc Magnets) — loose high-powered magnets exceeding flux limits and fitting CPSC's small-parts cylinder.
• Recall 26515 (Anzmtosn / Shenzhen Bangduola Luminous Fidget Spinner Balls on Amazon), Recall 26514 (Missry Associates' Misco Sports Light-Up Racket Sets), Recall 26483 (Misco Sports Badminton Toy Sets), Recall 26497 (ABC Trading children's toys), and Recall 26503 (ABC Trading WSDZ Light-up Glasses) — all cite accessible button-cell compartments.
• Recalls 26510 and 26484 pull loose lithium coin batteries from importer Proudly American Store (Canada) and Guangzhou Lichengbei Battery Technology (LiCB, sold on Amazon) for failing Reese's Law's child-resistant packaging and warning-label requirements.

Burn, fire, and impact hazards

• Recall 26513 — Zhejiang Mingrui Furniture (Joy Furniture) Talan and Royce living-room sets feature LED illuminated spheres that can overheat, mirroring Recall 26504 for Bethlehem Lights' 10-inch Illuminated Ribbon Spheres sold by QVC.
• Recall 26511 removes Tzumi Electronics SLF Sauna Blankets for overheating; Recall 26506 covers Giantex/Costway portable steam saunas whose diffuser sits too close to the user.
• Recall 26512 — Giantex lounge chairs carry a finger-pinch amputation hazard at the adjustment mechanism.
• Recall 26498 (HomeProGym resistance bands) and Recall 26486 (Amazon Basics 55-lb adjustable dumbbells) both cite impact hazards from components separating mid-exercise.

FDA — Drugs and Devices

Lead: Class I

• D-0553-2026 — Wisconsin Pharmacal Company is recalling MG217 Multi-Symptom Treatment Cream & Skin Protectant (colloidal oatmeal 2%, 6 oz, manufactured at Pharmacal, Jackson, WI) as Class I after confirmed *Staphylococcus aureus* contamination in the non-sterile product; recall initiated 2026-04-24.

Class II — sterility, nitrosamine, and labeling failures

• D-0546-2026 — UCB Biosciences is recalling Cimzia (certolizumab pegol) 2×200 mg/mL prefilled syringes (NDC 50474-710-79/-80/-81, including the Starter Kit and professional samples) for lack of sterility assurance.
• D-0545-2026 and D-0544-2026 — Zydus Pharmaceuticals (USA) is pulling Erythromycin Tablets USP 500 mg (NDC 70710-1048-3) and 250 mg (NDC 70710-1047-3), manufactured at Zydus Lifesciences, Ahmedabad, after CGMP deviations produced N-Nitroso-Desmethyl-Erythromycin above acceptable intake limits.
• D-0541-2026 — Lupin Pharmaceuticals is recalling Liraglutide Injection 18 mg/3 mL pen cartridges (NDC 70748-346-02 and -346-03, manufactured at Lupin Limited, Nagpur) over white thread-like particulate matter found in the cartridge.
• D-0548-2026 — IntegraDose Compounding Services (Shoreview, MN) is recalling sterile CADD fentanyl citrate 2,250 mcg/50 mL (NDC 71139-6030-1) as subpotent.
• D-0538-2026 — Safecor Health is recalling unit-dose atomoxetine HCl capsules (NDC 64380-474-01) after 25 mg capsules were labeled as 10 mg — a dose mix-up risking 2.5× overdose in ADHD patients.

Class III — Primidone cross-contamination cluster

Three concurrent recalls flag the same Lannett-sourced primidone API contaminated with trace Acemetacin (an NSAID API not approved in the U.S.):

• D-0537-2026 — American Health Packaging Primidone Tablets USP 50 mg unit-dose blisters (carton NDC 68084-202-01).
• D-0534-2026 — GSMS/Golden State Medical Supply Primidone Tablets USP 50 mg, 50-count (NDC 51407-637-05).
• D-0535-2026 — GSMS/Golden State Medical Supply Primidone Tablets USP 250 mg, 100-count (NDC 51407-638-01).