Consumer Recalls Daily — 2026-05-31

TITLE: Recalls Daily — Magnet & button-cell toy sweep dominates CPSC; FDA posts 10 Class II drug actions

---

CPSC — Consumer Products

Children's products: a magnet- and button-cell ingestion wave

The Commission's late-May docket is heavily weighted toward pediatric ingestion hazards, with multiple importers cited for violating the mandatory toy and button-cell standards under Reese's Law.

• High-powered magnet ingestion drove two violation-based recalls: 26509 covers Daoen's *Zen Magnetic Promotional Ball Sets*, and 26508 covers *MiniWarGaming and Primal Horizon Disc Magnets* (importer MiniWarGaming) — both fit within CPSC's small-parts cylinder and exceed permitted flux, posing a deadly ingestion hazard.
• Button-cell ingestion hazards account for five separate actions: 26515 (Anzmtosn / Shenzhen Bangduola luminous fidget spinner balls on Amazon), 26514 and 26483 (Missry Associates' Misco Sports light-up rackets and badminton sets, with battery covers that detach or unscrew), 26497 (ABC Trading children's toys), and 26503 (ABC Trading WSDZ light-up glasses, which also violate packaging rules).
• Standalone coin batteries were pulled twice for failing Reese's Law child-resistant packaging and labeling requirements: 26510 (Proudly American Store, Canada) and 26484 (LiCB / Guangzhou Lichengbei, sold on Amazon).
• 26499 Orb Funkee squeeze toys, imported by The Orb Factory, were recalled after testing found fibrous tremolite asbestos in the play sand — a rare carcinogen call-out on a children's product, with consumers told to remove the toys from children immediately.

Nursery, furniture and tip-over hazards

• 26522 Walmart is recalling *Mainstays 9-Drawer Fabric Dressers* (made by Hop Thang Interior Wood Co., Vietnam) for violating the STURDY Act clothing-storage stability standard; unanchored units pose tip-over and entrapment hazards that can kill children.
• 26502 PandaEar portable hook-on chairs violate the mandatory standard because the crotch restraint can be removed without a tool, allowing infants to fall through.
• 26493 Cosyland children's tower stools (imported by Cosyland Official) and 26490 Guidecraft children's standing towers were both recalled for collapse/fall hazards; the Cosyland units additionally allow torso entrapment through side openings.

Fire, burn and carbon-monoxide risks

• 26494 Generac Power Systems expanded its recall of Generac and DR Power electric-start pressure washers to additional models after the start/stop button was found to self-start the engine — a confirmed CO poisoning risk if used in enclosed spaces.
• 26513 Joy Furniture (Zhejiang Mingrui) *Talan* and *Royce* living-room sets and 26504 Bethlehem Lights 10-inch illuminated ribbon spheres (sold on QVC) were both recalled because integrated LED light assemblies can overheat and ignite.
• 26511 Tzumi Electronics SLF sauna blankets can overheat (fire/burn), and 26506 Giantex/Costway portable steam saunas can direct steam onto the user's skin.

Powered vehicles and adult equipment

• 26482 BRP is recalling Can-Am ATVs after the Speed Limiter Mode was found to malfunction and cause unexpected acceleration; owners are told to stop using Speed Limiter Mode pending a fix — a death-risk hazard for a major-brand off-road vehicle.
• 26501 Lil Pick Up youth ATVs fail the federal ATV standard on suspension and reverse-light requirements, posing crash and burn hazards.
• 26486 Amazon's *Amazon Basics 55-lb. Adjustable Dumbbells* and 26498 HomeProGym resistance bands were both pulled as impact hazards after weight plates or handles separated mid-use.
• 26512 Giantex lounge chairs were recalled for an amputation-risk pinch point in the adjustment mechanism, and 26479 Minka Lighting Group *Bardon Series* pendant fixtures can detach from the downrod during installation — an overhead impact hazard.

FDA — Drugs and Medical Devices

No Class I actions appear in today's batch; all ten postings are Class II, firm-initiated voluntary recalls, but several touch high-volume prescription products.

Sterility and contamination

• D-0525-2026 OASIS Medical is recalling *Oasis Tears PF Preservative-Free Lubricant Eye Drops* (10 mL, NDC 42126-6400-1, made in France) for lack of sterility assurance after FDA inspection findings at contract manufacturer Excelvision.
• D-0518-2026 and D-0517-2026 cover CareFusion 213 (BD) *PurPrep* povidone-iodine/IPA surgical prep applicators (10.5 mL and 26 mL sizes, NDC 54365-014-42 for the latter) — both pulled for potential contamination and lack of sterility assurance.
• D-0524-2026 Central Admixture Pharmacy Services (CAPS) Los Angeles recalled a patient-specific 1,660 mL TPN bag (Rx# 11-4909703-0-1) after it was compounded without the labeled insulin component — a formulation error with direct dosing implications.
• D-0527-2026 Endo USA is recalling *Buprenorphine HCl Injection* 0.3 mg/mL, 5×1 mL single-dose vials (NDC 42023-179-05) for particulate matter identified as buprenorphine free base.

Impurities, degradation and dissolution failures

• Ajanta Pharma (India) is recalling two strengths of *Duloxetine Delayed-Release Capsules* — D-0514-2026 (30 mg; NDCs 27241-098-09/-03/-10) and D-0516-2026 (20 mg; NDC 27241-097-06) — after N-nitroso-duloxetine exceeded the FDA's 0.83 ppm limit at 12- and 18-month stability points, the latest nitrosamine action against an SSRI/SNRI line.
• D-0523-2026 Acella Pharmaceuticals' *Naproxen Oral Suspension* 125 mg/5 mL (16 fl oz, NDC 42192-619-16, made in Canada) was recalled for lead and lithium above specification — a notable heavy-metal contamination call in a pediatric-friendly liquid analgesic.
• D-0520-2026 Rising Pharma / J.B. Chemicals (Unique Pharmaceutical Labs, Mumbai) is recalling *Enalapril Maleate Tablets* 20 mg in 1,000-count bottles for out-of-spec organic impurities.
• D-0547-2026 Ascend Laboratories / Alkem (India) recalled *Metoprolol Succinate ER Tablets* 25 mg (NDC 67877-590-01) for failed dissolution — relevant for cardiac patients dependent on the extended-release profile.