Consumer Recalls Daily — 2026-05-24

TITLE: Recalls Daily — May 24: Can-Am ATV death-risk recall leads CPSC sweep; duloxetine nitrosamine cluster dominates FDA

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CPSC — Consumer Products

Lead: Death-and-injury hazards

• [26482] BRP is recalling Can-Am ATVs after the speed limiter control was found to malfunction and trigger unexpected acceleration — CPSC flags a serious risk of injury or death from crash hazard, and consumers are told to stop using Speed Limiter Mode immediately pending repair.
• [26494] Generac Power Systems (Waukesha, WI) is expanding its recall of Generac and DR Power electric-start pressure washers to additional models after reports the electronic start/stop button can self-actuate, posing a fatal carbon-monoxide risk if a unit runs in a confined space.
• [26484] LiCB lithium coin batteries, imported by Guangzhou Lichengbei Battery Technology and sold on Amazon, were sold without the child-resistant packaging and warning labels required under Reese's Law — a federal statute violation tied to ingestion deaths in young children.
• [26479] Minka Lighting Group's Bardon Series pendant light fixtures can detach from the downrod during installation, dropping the frame onto installers — CPSC cites impact-hazard risk of serious injury or death.

Climbing and fall-protection harnesses

Petzl America issued two separate recalls of professional fall-protection harnesses on May 14, both flagged for death-risk fall hazards:

• [26488] ASTRO BOD FAST, ASTRO SIT FAST, and CANYON GUIDE harnesses can have the D-ring release, opening the primary attachment point.
• [26487] SIMBA and SWAN EASYFIT harnesses are missing rivets in the FAST LT PIN-LOCK buckles, which can open under load. Work-at-height professionals and operators are told to stop use and sale immediately.

Children's products (Reese's Law, toy-safety, and furniture stability)

• [26493] Cosyland tower stools (imported by Cosyland Official) can collapse or tip, with front/back openings large enough for a child's torso — CPSC cites tip-over, fall, and entrapment death risk. [26490] Guidecraft's children's standing towers are separately recalled because the inner platform can loosen and detach.
• [26448] UHOMEPRO 5-drawer dressers violate the mandatory STURDY-Act clothing storage standard, posing tip-over and entrapment death hazards if not anchored.
• Button-cell ingestion cluster: [26483] Missry Associates' Misco Sports Badminton Toy Sets (button cells in the shuttlecocks), [26466] ZMC Group's light-up toys, and [26465] EEMB USA battery pouches all fail either the toys standard or Reese's Law child-resistant packaging requirements.
• Other children's recalls: [26481] Tiyol pull-string teething toys (ZW Creations, Amazon) — silicone strings exceed length limits, choking risk; [26472] Justforjoyful Rainbow Wall Toys — xylophone drumstick has a spherical choking-hazard end; [26477] Allura Imports youth bobcat-logo sweatshirts — drawstrings violate federal upper-outerwear strangulation regs; [26469] Natural Pigments Rublev Colours gum turpentine and mineral spirits lack child-resistant packaging required under the Poison Prevention Packaging Act.
• Helmets failing the bicycle-helmet standard: [26467] Favoto bicycle helmets (Amazon) and [26470] Foubeaka/Geniuss multi-purpose helmets (Temu) — neither meets positional stability or certification requirements.

Home, fitness, and other goods

• [26486] Amazon Basics 55-lb adjustable dumbbells are recalled because weight plates can fail to engage and fly off the handle during use — impact hazard.
• [26489] ZWILLING J.A. Henckels (Solingen, Germany) electric water kettles can have the handle loosen and separate, spilling boiling water — burn hazard.
• [26485] World Bright International's Agio Menlo woven patio swings, sold at Costco, can have the seat detach from the frame mid-use — fall hazard with death risk.
• [26480] Superbobi pool drain covers (manufactured by Shenzhen Jiangtou Technology, dba Remy&shop) violate the Virginia Graeme Baker Pool & Spa Safety Act for entrapment protection — drowning hazard.
• [26468] Svnntaa adult portable bed rails (Eokeanon, Amazon) fail the mandatory standard, with documented entrapment/asphyxiation risk between rail and mattress.
• [26478] EVLWZL and Gunugu mattresses fail the mandatory mattress flammability standard — fire-death risk.
• [26475] Analemma water bottles (New Earth Technologies d.o.o.) have an inner glass liner that can shatter, posing laceration and ingestion hazards.

FDA — Drugs and Devices

Lead: Duloxetine nitrosamine cluster (Class II)

Three concurrent Class II recalls were initiated around April 21–29 for N-nitroso-duloxetine impurity above FDA's 0.83 ppm limit, identified at 12- and 18-month long-term stability intervals:

• [D-0514-2026] Ajanta Pharma duloxetine DR capsules, 30 mg, NDCs 27241-098-09/03/10.
• [D-0516-2026] Ajanta Pharma duloxetine DR capsules, 20 mg, NDC 27241-097-06.
• [D-0522-2026] Breckenridge Pharmaceutical duloxetine DR capsules, 60 mg, NDC 51991-748-90 (manufactured by Towa Pharmaceutical Europe in Spain). The cluster suggests a broader nitrosamine surveillance issue across multiple duloxetine API sources.

Other drug recalls (all Class II unless noted)

• [D-0524-2026] Central Admixture Pharmacy Services (CAPS, Los Angeles) recalled a patient-specific TPN bag (Rx# 11-4909703-0-1, 1660 mL) that was compounded without the insulin listed on the label — a formulation error in a refrigerated single-dose injection.
• [D-0523-2026] Acella Pharmaceuticals' naproxen oral suspension 125 mg/5 mL, 473 mL bottles (NDC 42192-619-16), recalled for lead and lithium above specification — chemical contamination in a pediatric-friendly liquid formulation.
• [D-0520-2026] Enalapril maleate 20 mg tablets, 1,000-count, manufactured by Unique Pharmaceutical Laboratories (J.B. Chemicals, Mumbai) for Rising Pharma — out-of-spec organic impurities result.
• [D-0511-2026] Class III — Unichem Pharmaceuticals buspirone HCl 5 mg tablets, 500-count, recalled as subpotent.

Devices and infusion products

• [D-0517-2026] and [D-0518-2026] CareFusion 213 (a Becton Dickinson subsidiary, El Paso, TX) recalled two configurations of BD PurPrep povidone-iodine/IPA sterile applicators (NDC 54365-014-42 among them) for lack of sterility assurance — potential product contamination in a pre-surgical antiseptic.
• [Class Not Yet Classified] B. Braun Medical's Lactated Ringer's Injection USP, 1000 mL (NDC 0264-7750-07) was recalled April 28 for particulate matter; classification still pending.