Consumer Recalls Daily — 2026-05-22

TITLE: Recalls Daily — Can-Am ATVs, Generac pressure washers, Petzl harnesses lead death-risk wave; duloxetine nitrosamine sweep widens

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CPSC — Consumer Products

The May 14 docket is dominated by death-risk recalls across motorized equipment, fall-protection gear, and children's products. Reese's Law and the toy safety standard continue driving a steady current of button-cell and choking enforcement actions against Amazon and Temu third-party sellers.

Lead: Injury- and Death-Risk Recalls

• BRP Can-Am ATVs (recall 26482) are being recalled after the Speed Limiter Mode control can malfunction and cause unexpected acceleration; BRP is directing owners to stop using the limiter immediately pending a fix — crash hazard with risk of serious injury or death.
• Generac Power Systems is expanding its earlier recall of Generac and DR Power electric-start pressure washers (26494) to additional models after the electronic start/stop button can self-actuate, posing a carbon-monoxide poisoning risk if the unit starts in a confined space.
• Petzl America issued two simultaneous fall-protection recalls: ASTRO BOD FAST, ASTRO SIT FAST and CANYON GUIDE harnesses (26488) whose D-ring can release, and SIMBA and SWAN EASYFIT harnesses (26487) missing rivets in their FAST LT PIN-LOCK buckles — both flagged as risk of serious injury or death to work-at-height and rescue professionals.
• Minka Lighting Group's Bardon Series pendant fixtures (26479) can have the frame detach from the downrod during installation, an impact hazard the agency rates at serious-injury-or-death severity.
• Agio Menlo Woven patio swings, imported by World Bright International and sold at Costco (26485), can have the seat detach from the frame mid-use; consumers are told to stop using immediately.
• ZWILLING J. A. Henckels is recalling electric water kettles (26489) whose handles can loosen and separate, spilling boiling contents — burn hazard.
• Amazon Basics 55-lb. adjustable dumbbells (26486) can fail to engage weight plates that then dislodge mid-lift, an impact hazard Amazon is addressing through its standard recall process.

Children's Products — Recurring Patterns

• Two children's "tower stool" recalls landed the same day: Cosyland tower stools (26493) can collapse, tip, or entrap a child's torso through front/back openings, and Guidecraft standing towers (26490) have platforms that loosen and detach over time — both death-or-serious-injury rated.
• UHOMEPRO 5-drawer dressers (26448) violate the STURDY Act clothing-storage stability standard, presenting tip-over and entrapment hazards if not anchored.
• Svnntaa adult portable bed rails sold on Amazon by Eokeanon (26468) violate the mandatory bed-rail standard, with entrapment and asphyxiation risk between rail and mattress.
• Allura Imports youth Bobcat-logo sweatshirts (26477) carry drawstrings in violation of the federal children's upper-outerwear rule — strangulation hazard.

Button-Cell / Reese's Law Sweep

A coordinated cluster of battery-ingestion recalls hit this cycle: LiCB (Guangzhou Lichengbei) lithium coin batteries sold on Amazon (26484) and EEMB USA battery pouches (26465) both lack the child-resistant packaging required under Reese's Law; Missry Associates Misco Sports badminton sets (26483) and ZMC Group light-up toys (26466) violate the toy standard by allowing easy access to button cells.

Toy, Helmet, and Other Standard Violations

• Favoto bicycle helmets sold on Amazon (26467) and Foubeaka/Geniuss multi-purpose helmets sold on Temu (26470) both fail the mandatory positional-stability and certification requirements of the bicycle helmet standard.
• Tiyol pull-string teething toys sold by ZW Creations on Amazon (26481) have silicone strings longer than permitted, creating a choking/airway-obstruction risk; Justforjoyful Rainbow Wall toys (26472) have a spherical drumstick end posing a choking hazard.
• EVLWZL and Gunugu mattresses (26478) fail the federal mattress flammability standard — fire hazard.
• Superbobi pool drain covers manufactured by Shenzhen Jiangtou (Remy&shop) (26480) violate the Virginia Graeme Baker Pool & Spa Safety Act, presenting entrapment and drowning hazards.
• Analemma water bottles imported by New Earth Technologies (26475) can have the inner glass liner shatter, causing laceration and ingestion risk.
• Natural Pigments Rublev Colours gum turpentine and mineral spirits (26469) lack the child-resistant packaging required under the Poison Prevention Packaging Act.

FDA — Drugs and Devices

No Class I actions this cycle; one Class III and one not-yet-classified, with Class II accounting for the balance. The standout pattern is a multi-firm N-nitroso-duloxetine nitrosamine sweep hitting three different distributors of duloxetine delayed-release capsules.

Nitrosamine Cluster — Duloxetine DR Capsules

• Ajanta Pharma Ltd. is recalling duloxetine DR 30 mg capsules (D-0514-2026, NDC 27241-098-03/-09/-10) and 20 mg capsules (D-0516-2026, NDC 27241-097-06) after 12- and 18-month stability testing found N-nitroso-duloxetine above FDA's 0.83 ppm limit — Class II, CGMP deviation.
• Breckenridge Pharmaceutical is recalling duloxetine DR 60 mg, 90-count (D-0522-2026, NDC 51991-748-90), manufactured by Towa Pharmaceutical Europe in Spain, for the same nitrosamine impurity — Class II.

Other Drug Recalls

• Acella Pharmaceuticals' naproxen oral suspension 125 mg/5mL, 473 mL bottles (D-0523-2026, NDC 42192-619-16), is Class II for chemical contamination — lead and lithium above specification — a notable contamination flag for a pediatric-dosing liquid.
• CAPS (Central Admixture Pharmacy Services), Los Angeles recalled a patient-specific TPN bag, Rx# 11-4909703-0-1, 1660 mL (D-0524-2026) after the compounded product did not contain insulin as labeled — Class II, incorrect formulation.
• JB Chemicals / Unique Pharmaceutical Labs enalapril maleate 20 mg tablets, 1,000-count, distributed by Rising Pharma (D-0520-2026), recalled Class II for an out-of-specification organic-impurities result.
• Unichem Pharmaceuticals buspirone HCl 5 mg, 500-count bottle (D-0511-2026) is Class III for subpotency — the only Class III this cycle.

Devices and Sterile Products

• CareFusion 213 (BD) PurPrep povidone-iodine/IPA sterile applicators are recalled in two presentations — 10.5 mL applicators, 25/box (D-0518-2026) and 26 mL applicators, NDC 54365-014-42 (D-0517-2026) — both Class II for lack of sterility assurance.
• B. Braun Medical Lactated Ringer's Injection USP, 1000 mL, NDC 0264-7750-07 (classification pending) was recalled for particulate matter; class designation has not yet been assigned by FDA.