Consumer Recalls Daily — 2026-05-29

TITLE: Recalls Daily — Magnet, button-cell hazards dominate CPSC sweep; FDA flags duloxetine nitrosamine, lead in naproxen suspension

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CPSC — Consumer Products

The May 28 CPSC bulletin is dominated by ingestion and fire-hazard recalls aimed at children's products, with multiple deadly-hazard citations and a renewed enforcement push around Reese's Law button-cell packaging requirements.

Lead: Risk of serious injury or death

• Recall 26509 — Daoen pulled its Zen Magnetic Promotional Ball Sets after the loose high-powered magnets were found to violate the mandatory toy standard, posing a fatal ingestion hazard when multiple magnets attract across bowel tissue.
• Recall 26508 — MiniWarGaming recalled its MiniWarGaming and Primal Horizon disc magnets for the same defect: the magnets fit inside CPSC's small-parts cylinder and exceed allowable flux strength, violating the mandatory magnet standard.
• Recall 26522 — Walmart recalled Mainstays 9-Drawer Fabric Dressers (made by Vietnam's Hop Thang Interior Wood) for failing the STURDY Act clothing-storage-unit standard; the unanchored dressers pose tip-over and entrapment risks fatal to children.
• Recall 26502 — PandaEar Portable Hook-On Chairs were recalled after testing showed the crotch restraint could be removed without a tool, allowing infants to slip through and fall — a violation of the mandatory hook-on chair standard.
• Recall 26499 — The Orb Factory recalled Orb Funkee Squeeze Toys because the sand inside may contain fibrous tremolite asbestos, a rare but serious inhalation-exposure citation.
• Recall 26494 — Generac expanded its earlier recall of Generac and DR Power electric-start pressure washers (Waukesha, WI) to additional models after reports that the start/stop button can self-actuate, posing a fatal carbon-monoxide risk in enclosed spaces.
• Recall 26482 — BRP recalled Can-Am youth ATVs after the speed-limiter control was found to malfunction and allow unintended acceleration; consumers are told to stop using Speed Limiter Mode pending repair.
• Recall 26501 — Lil Pick Up recalled youth ATVs that fail the mandatory ATV standard on mechanical suspension and reverse-indicator illumination, posing crash and burn hazards.

Button-cell battery cluster (Reese's Law enforcement)

A coordinated set of recalls targets toys and batteries that violate the federal child-resistant packaging and access-prevention rules for button cells:

• Recalls 26515, 26514, 26497, 26503, 26483 cover Anzmtosn Luminous Fidget Spinner Balls (sold on Amazon by Shenzhen Bangduola), Missry Associates' Misco Sports Light-Up Racket Sets and Badminton Toy Sets, and two ABC Trading lines (children's toys and WSDZ Light-up Glasses) — all cited for accessible button-cell compartments under the mandatory toy or button-cell consumer-product standards.
• Recalls 26510 and 26484 target loose lithium coin batteries themselves: Canada's Proudly American Store and China's Guangzhou Lichengbei Battery Technology (LiCB, sold on Amazon) shipped cells without child-resistant packaging or Reese's Law warning labels.

Fire, burn, and impact hazards

• Recall 26513 — Zhejiang Mingrui Furniture (Joy Furniture) recalled Talan and Royce living-room sets after the LED-illuminated spheres were found to overheat; Recall 26504 flags the same defect in Bethlehem Lights' 10-inch Illuminated Ribbon Spheres sold by QVC.
• Recalls 26511 and 26506 — Tzumi Electronics SLF Sauna Blankets can overheat (fire/burn), and Giantex portable steam saunas (sold under Giantex and Costway) position the steam diffuser close enough to scald users.
• Recall 26479 — Minka Lighting's Bardon Series pendant fixtures can detach from the downrod during installation, an impact hazard with fatal potential.
• Recall 26512 — Giantex lounge chairs contain a finger pinch point during adjustment, cited as an amputation hazard.

Children's furniture and fitness gear

• Recalls 26493 and 26490 — Cosyland tower stools (sold via Cosyland Official) can collapse with torso-sized openings front and back, and Guidecraft standing towers can loosen at the platform — both cited as fall/entrapment hazards to toddlers.
• Recalls 26498 and 26486 — HomeProGym resistance bands can separate from the handle mid-rep, and Amazon Basics 55-lb adjustable dumbbells can shed plates during weight changes; both are impact-hazard recalls aimed at home-gym users.

FDA — Drugs and Devices

All ten FDA actions this cycle are Class II, firm-initiated voluntary recalls — no Class I in the batch — but several involve impurities and contamination relevant to long-term safety.

Impurity and contamination

• Recalls D-0514-2026 and D-0516-2026 — Ajanta Pharma (Bridgewater, NJ; made in India) is pulling Duloxetine Delayed-Release Capsules 30 mg (NDC 27241-098-09/-03/-10) and 20 mg (NDC 27241-097-06) after N-nitroso-duloxetine was detected above FDA's 0.83 ppm limit at the 12- and 18-month stability intervals — the latest nitrosamine hit in the SSRI/SNRI category.
• Recall D-0523-2026 — Acella Pharmaceuticals recalled Naproxen Oral Suspension USP 125 mg/5 mL in 473 mL bottles (NDC 42192-619-16, made in Canada) for lead and lithium contamination above specification, notable because the suspension formulation is commonly dispensed to pediatric patients.
• Recall D-0527-2026 — Endo USA recalled Buprenorphine HCl Injection 0.3 mg/mL, 5×1 mL single-dose vials (NDC 42023-179-05) after particulate matter identified as buprenorphine free base was found in finished product.
• Recalls D-0520-2026 and D-0547-2026 — Rising Pharma's Enalapril Maleate 20 mg tablets (made by Unique Pharmaceutical/JB Chemicals, Mumbai) failed organic-impurities testing, and Ascend Laboratories' Metoprolol Succinate ER 25 mg (NDC 67877-590-01, made by Alkem in India) failed dissolution — two cardiovascular generics with potency/quality concerns.

Sterility

• Recall D-0525-2026 — OASIS Medical (Glendora, CA) recalled Oasis Tears PF preservative-free lubricant eye drops, 10 mL bottles (NDC 42126-6400-1), made in France by Excelvision, citing lack of sterility assurance after FDA inspection observations.
• Recalls D-0518-2026 and D-0517-2026 — CareFusion 213 (a Becton Dickinson subsidiary, El Paso TX) recalled two BD PurPrep povidone-iodine/IPA antiseptic configurations (10.5 mL and 26 mL applicators, NDC 54365-014-42) over potential contamination — a notable surgical-prep alert.
• Recall D-0524-2026 — Central Admixture Pharmacy Services (CAPS) Los Angeles recalled a patient-specific TPN bag (Rx# 11-4909703-0-1, 1660 mL) after the compounded product was found to lack the labeled insulin — a compounding-formulation error.