Consumer Recalls Daily — 2026-05-30

TITLE: Recall Digest 2026-05-30: Magnet & button-cell toys dominate CPSC action; FDA logs duloxetine nitrosamine, naproxen lead contamination

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CPSC — Consumer Products

The dominant theme across the May 14, May 21, and May 28 CPSC drops is pediatric ingestion: high-powered magnets, loose button-cell batteries, and unsecured battery compartments account for roughly half of all recalls cited with risk of serious injury or death.

Lead actions — serious injury or death risk

• #26509 Daoen's Zen Magnetic Promotional Ball Sets are recalled as loose high-powered magnets that violate the federal mandatory toy standard; if swallowed they attract through tissue and can perforate the intestines.
• #26508 MiniWarGaming and Primal Horizon disc magnets, imported by MiniWarGaming, exceed the flux-index limit and fit within the small-parts cylinder — another deadly-ingestion recall under the magnets rule.
• #26510 / #26484 Two separate lithium coin-battery recalls (Proudly American Store of Canada; LiCB / Guangzhou Lichengbei Battery Technology, sold on Amazon) cite missing child-resistant packaging and absent Reese's Law warnings.
• #26515 Anzmtosn (Shenzhen Bangduola) Luminous Fidget Spinner Balls and #26514 / #26483 Missry Associates' Misco Sports light-up racket and badminton toy sets were recalled because button cells in shuttlecocks and handles can be accessed by children — all violate the mandatory toys standard.
• #26497 / #26503 ABC Trading pulled both its children's toys line and WSDZ light-up glasses for the same button-cell access failure.
• #26522 Walmart recalled Mainstays 9-Drawer Fabric Dressers (made by Hop Thang Interior Wood, Vietnam) for tip-over and entrapment hazards; the units fail the mandatory CSU stability standard. Tip-overs have killed children before — treat as a high-priority household sweep.
• #26502 PandaEar Portable Hook-On Chairs violate the hook-on-chair standard because the crotch restraint can be removed without a tool, allowing infants to fall through.
• #26499 Orb Funkee Squeeze Toys, imported by The Orb Factory, may contain fibrous tremolite asbestos in the play sand — a rare asbestos-in-toy recall warranting immediate removal from children.
• #26494 Generac Power Systems expanded its recall of Generac and DR Power electric-start pressure washers (Waukesha, WI): the start button can self-trigger, posing a CO poisoning death risk in enclosed spaces. Owners of earlier-listed units should re-check serials against the expanded scope.
• #26501 Lil Pick Up youth ATVs fail the mandatory ATV standard (suspension and reverse-light defects); #26482 BRP Can-Am ATVs have a malfunctioning speed limiter that can cause unintended acceleration — BRP advises immediately ceasing use of Speed Limiter Mode pending repair.
• #26493 Cosyland children's tower stools (Cosyland Official) can collapse or allow torso entrapment through side openings, and #26490 Guidecraft standing towers can have the inner platform detach — two similar Montessori-style tower recalls in the same drop.

Fire, burn, and impact hazards

• #26513 Joy Furniture (Zhejiang Mingrui) recalled Talan and Royce illuminated living-room furniture sets because the embedded LED spheres can overheat — paired thematically with #26504 Bethlehem Lights' 10-inch Illuminated Ribbon Spheres sold by QVC, recalled for the same overheating failure.
• #26511 Tzumi Electronics SLF Sauna Blankets and #26506 Giantex/Costway Portable Steam Saunas were both pulled for overheating/burn hazards — consumers should stop use and seek replacement (Tzumi) or refund (Giantex).
• #26479 Minka Lighting Group's Bardon Series pendant fixtures can detach from the downrod during installation, an impact-hazard recall.
• #26512 Giantex lounge chairs have an adjustment pinch point cited as an amputation hazard.
• #26486 Amazon Basics 55-lb adjustable dumbbells and #26498 HomeProGym resistance bands round out a fitness-equipment cluster: plates can dislodge mid-lift and bands can separate from handles, both impact hazards.

FDA — Drugs

No Class I recalls this cycle; all ten posted enforcement entries are Class II (temporary or medically reversible adverse-event risk), firm-initiated.

Notable themes

• Nitrosamine impurity in duloxetine. Ajanta Pharma Ltd. (Bridgewater, NJ marketer; made in India) initiated two parallel recalls — D-0514-2026 for Duloxetine DR Capsules 30 mg (NDC 27241-098-09/-03/-10) and D-0516-2026 for the 20 mg strength (NDC 27241-097-06) — after N-nitroso-duloxetine exceeded the FDA's 0.83 ppm limit at 12- and 18-month stability pulls. Pharmacies dispensing Ajanta-sourced duloxetine should pull stock and check for affected NDCs.
• Heavy-metal contamination in a pediatric-adjacent product. D-0523-2026 — Acella Pharmaceuticals' Naproxen Oral Suspension 125 mg/5 mL, 473 mL bottles (NDC 42192-619-16, made in Canada) — was recalled for lead and lithium above specification. Oral suspensions are commonly used in pediatric and geriatric dispensing; review on-hand inventory.
• Sterility assurance failures. D-0525-2026 Oasis Tears PF preservative-free eye drops (OASIS Medical, Glendora CA; NDC 42126-6400-1) were pulled following FDA inspection observations at French manufacturer Excelvision. D-0518-2026 and D-0517-2026 cover two pack configurations of CareFusion 213's BD PurPrep povidone-iodine/IPA surgical applicators (El Paso, TX; NDC 54365-014-42 for the 26 mL carton) for potential contamination.
• Compounding error. D-0524-2026 — a patient-specific TPN bag (Rx# 11-4909703-0-1, 1,660 mL) from Central Admixture Pharmacy Services, Santa Fe Springs CA, was recalled because the compounded product did not contain insulin as labeled. Single-patient scope but a notable formulation-error event for CAPS.
• Particulate, dissolution, and impurities failures. D-0527-2026 Endo USA's Buprenorphine HCl injection 0.3 mg/mL (NDC 42023-179-05) was recalled for buprenorphine free-base particulates; D-0547-2026 Ascend Laboratories' metoprolol succinate ER 25 mg (made by Alkem, India; NDC 67877-590-01) failed dissolution; D-0520-2026 Rising Pharma's enalapril maleate 20 mg 1,000-count (made by Unique Pharmaceutical/JB Chemicals, Mumbai) failed organic-impurities specification.

Devices / Food

No FDA device or food recalls in today's feed.