Consumer Recalls Daily — 2026-06-01

TITLE: Consumer Recalls Daily — Magnet, battery and tip-over hazards dominate CPSC slate; FDA logs sterility and nitrosamine actions

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CPSC — Consumer Goods

Lead: Children's product hazards with risk of serious injury or death

A wave of CPSC actions on May 21 and May 28 targets ingestion, fire and fall hazards in children's products, several explicitly citing risk of death.

• 26509 — Daoen recalled Zen Magnetic Promotional Ball Sets after the loose high-powered magnets failed the mandatory toy standard, posing a fatal ingestion hazard if multiple magnets attract through the intestinal wall.
• 26508 — MiniWarGaming and Primal Horizon disc magnets were recalled because the high-powered magnets fit inside CPSC's small-parts cylinder and exceed allowable flux, violating the mandatory magnet standard.
• 26499 — The Orb Factory's Orb Funkee squeeze toys were pulled after sand fill was found to contain fibrous tremolite asbestos, an inhalation hazard for children; consumers are told to remove the toys from children immediately.
• 26515, 26514, 26497, 26503, 26483 — A cluster of toy recalls (Anzmtosn Luminous Fidget Spinner Balls on Amazon, Missry Associates' Misco Sports light-up rackets and badminton sets, and two ABC Trading actions covering children's toys and WSDZ light-up glasses) all cite easily accessible button-cell batteries in violation of the mandatory toys or button-cell battery standards.
• 26510, 26484 — Lithium coin batteries imported by Proudly American Store (Canada) and by LiCB / Guangzhou Lichengbei (sold on Amazon) were recalled for lacking child-resistant packaging and Reese's Law warning labels.

Tip-over, fall and entrapment hazards for children

• 26522 — Walmart recalled Mainstays 9-Drawer Fabric Dressers (made by Hop Thang Interior Wood Co., Vietnam) after they failed the mandatory clothing storage unit stability standard, creating tip-over and entrapment hazards that can kill children when not anchored.
• 26502 — PandaEar portable hook-on chairs were recalled because the crotch restraint can be removed without a tool, allowing infants to fall through an opening in violation of the mandatory standard.
• 26493 — Cosyland Official children's tower stools can collapse or tip over, and a child's torso can fit through front and back openings, triggering recall over fall, tip-over and entrapment risks.
• 26490 — Guidecraft children's standing towers were recalled after the inside platform loosened over time, detaching and dropping young users.

Fire, burn and carbon-monoxide hazards

• 26513 — Joy Furniture (Zhejiang Mingrui) recalled Talan and Royce living-room sets after LED-illuminated spheres in the furniture overheated, posing a fire hazard with risk of serious injury or death.
• 26504 — Bethlehem Lights LLC (Naperville, Ill.) recalled 10-inch Illuminated Ribbon Spheres sold by QVC for the same overheating LED defect.
• 26494 — Generac Power Systems expanded its recall of Generac and DR Power electric-start pressure washers after additional models were found with start/stop buttons that can self-actuate, creating a fatal CO poisoning risk in enclosed spaces.
• 26511 — Tzumi Electronics recalled SLF Sauna Blankets for overheating that creates fire and burn hazards; consumers can obtain a replacement.
• 26506 — Giantex (and Costway-branded) portable steam saunas were recalled because the steam diffuser can sit too close to the user, causing burns.

Mechanical, impact and crash hazards

• 26482 — BRP recalled Can-Am ATVs after the Speed Limiter Mode control was found to malfunction and cause unexpected acceleration, citing a serious risk of injury or death; owners are told to stop using Speed Limiter Mode pending repair.
• 26501 — Lil Pick Up recalled youth ATVs that fail the mandatory ATV standard, including non-conforming mechanical suspension and a reverse indicator light that does not illuminate, creating crash and burn risks.
• 26512 — Giantex recalled lounge chairs after consumers' fingers could enter a pinch point during adjustment, posing an amputation hazard.
• 26479 — Minka Lighting Group recalled Bardon Series pendant fixtures whose frames can detach from the downrod during installation, creating an impact hazard with risk of death.
• 26486 — Amazon recalled Amazon Basics 55-lb Adjustable Dumbbells after weight plates were found to dislodge mid-lift, an impact hazard.
• 26498 — HomeProGym resistance bands were recalled because the band can forcefully separate from the handle during use.

FDA — Drugs and Medical Products

No Class I actions appear in today's FDA slate; all ten entries are Class II, firm-initiated recalls. The dominant themes are sterility assurance, nitrosamine impurities and dissolution/impurity out-of-specs.

Sterility-assurance actions

• D-0525-2026 — Oasis Medical (Glendora, Calif.) recalled Oasis Tears PF Preservative-Free Lubricant Eye Drops, 10 mL bottles, NDC 42126-6400-1 (made in France), out of an abundance of caution following FDA observations during an inspection of contract manufacturer Excelvision.
• D-0518-2026 / D-0517-2026 — CareFusion 213, LLC (El Paso, Texas; a Becton Dickinson subsidiary) recalled BD PurPrep povidone-iodine 8.3% / IPA 72.5% sterile applicators in both the 10.5 mL/25-applicator carton and the 26 mL/25-applicator carton (NDC 54365-014-42) for potential contamination.

Nitrosamine and impurity issues

• D-0514-2026 and D-0516-2026 — Ajanta Pharma Ltd. (India) recalled Duloxetine Delayed-Release Capsules 30 mg (NDC 27241-098-09/-03/-10) and 20 mg (NDC 27241-097-06) after 12- and 18-month stability samples showed N-nitroso-duloxetine above the FDA-recommended 0.83 ppm limit.
• D-0520-2026 — JB Chemicals/Unique Pharmaceutical Laboratories (Mumbai), distributed by Rising Pharma, recalled Enalapril Maleate 20 mg tablets in 1,000-count bottles for out-of-specification organic impurities.
• D-0547-2026 — Ascend Laboratories recalled Metoprolol Succinate ER 25 mg tablets (NDC 67877-590-01; manufactured by Alkem Laboratories, India) for failing dissolution specifications.
• D-0523-2026 — Acella Pharmaceuticals (Alpharetta, Ga.) recalled Naproxen Oral Suspension 125 mg/5 mL in 16 fl oz bottles (NDC 42192-619-16; made in Canada) after lead and lithium were detected above specification.

Particulates and compounding errors

• D-0527-2026 — Endo USA (Malvern, Pa.) recalled Buprenorphine HCl Injection 0.3 mg/mL, 5×1 mL single-dose vials (NDC 42023-179-05) for visible particulate matter identified as buprenorphine free base.
• D-0524-2026 — Central Admixture Pharmacy Services (CAPS) Los Angeles recalled a patient-specific TPN bag (Rx# 11-4909703-0-1, 1,660 mL) that was compounded without the insulin listed on the label — an incorrect-formulation event noteworthy given the dosing implications for the receiving patient.