Consumer Recalls Daily — 2026-05-28

TITLE: Recalls Daily — Button-cell battery sweep hits toys and packaging; CareFusion antiseptic and Ajanta duloxetine lead FDA actions

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CPSC — Consumer Products

Lead: Death-risk recalls

• Recall 26501 — Lil Pick Up is recalling youth ATVs that violate the federal mandatory ATV safety standard, with deficient mechanical suspension and a non-illuminating reverse indicator creating crash and burn hazards capable of causing death.
• Recall 26482 — BRP is recalling Can-Am ATVs because the Speed Limiter Mode control can malfunction and cause unexpected acceleration, posing a serious crash and fatality risk; owners should stop using Speed Limiter Mode immediately.
• Recall 26494 — Generac Power Systems is expanding its recall of Generac and DR Power electric-start pressure washers (Waukesha, WI) after the start/stop button can self-activate, posing a carbon-monoxide poisoning death hazard in enclosed spaces.
• Recall 26480 — Shenzhen Jiangtou Technology's Remy&shop "Superbobi" pool drain covers violate the Virginia Graeme Baker Pool & Spa Safety Act, posing entrapment and drowning hazards to swimmers.
• Recall 26485 — World Bright International is recalling Agio Menlo woven patio swings sold at Costco because the seat can detach from the frame mid-use, causing a potentially fatal fall.
• Recall 26478 — EVLWZL and Gunugu mattresses fail the federal mattress flammability standard, creating a fire hazard with risk of death.
• Recall 26504 — Bethlehem Lights LLC (Naperville, IL) is recalling 10-inch illuminated ribbon spheres sold by QVC after LEDs can overheat and ignite.

Button-cell battery cluster (Reese's Law)

CPSC issued five battery-related actions citing ingestion hazards that can cause internal chemical burns and death:

• Recalls 26497 and 26503 — ABC Trading is recalling unspecified children's toys and WSDZ light-up glasses; both violate the mandatory toy and consumer-product standards because button-cell battery compartments open without tools.
• Recall 26483 — Missry Associates' Misco Sports Badminton Toy Sets contain button-cell batteries in the shuttlecocks that are easily accessible to children, violating the mandatory toy safety standard.
• Recall 26484 — Guangzhou Lichengbei Battery Technology (dba LiCB), sold via Amazon, is recalling lithium coin cells distributed without child-resistant packaging or Reese's Law warning labels.
• Recall 26465 — EEMB USA is recalling battery pouches packaging lithium coin cells in non-child-resistant pouches in violation of Reese's Law.

Children's products — falls, choking, strangulation, asbestos

• Recall 26499 — Orb Funkee squeeze toys imported by The Orb Factory may contain fibrous tremolite asbestos in the play sand, posing inhalation risks; consumers should remove the toys from children immediately.
• Recall 26502 — PandaEar portable hook-on chairs violate the mandatory standard because the crotch restraint can be removed without tools, creating an opening through which infants can fall.
• Recall 26493 — Cosyland Official tower stools for children can collapse or tip, and openings on the front and back are large enough for a child's torso, posing entrapment and fall fatality risks.
• Recall 26490 — Guidecraft children's standing towers have an internal platform that can loosen over time and detach, causing falls.
• Recall 26481 — Tiyol pull-string teething toys, sold on Amazon by ZW Creations, have silicone strings longer than permitted that can reach the back of the throat and choke a child.
• Recall 26477 — Allura Imports youth sweatshirts with bobcat logo carry drawstrings that violate federal children's upper outerwear regulations, creating a strangulation hazard.

General consumer goods

• Recall 26486 — Amazon Basics 55-lb adjustable dumbbells can fail to fully engage weight plates, which then dislodge during use; Amazon is instructing buyers to stop using and follow its remedy steps.
• Recall 26498 — HomeProGym resistance bands can forcefully separate from their handles in use, creating a serious impact hazard.
• Recalls 26488 and 26487 — Petzl America is recalling two harness lines: ASTRO BOD FAST, ASTRO SIT FAST and CANYON GUIDE harnesses (D-ring can release, opening the attachment point) and SIMBA and SWAN EASYFIT harnesses (missing rivets in FAST LT PIN-LOCK buckles), both posing fall fatality risks for work-at-height users.
• Recall 26479 — Minka Lighting Group's Bardon Series pendant fixtures can have the frame detach from the downrod during installation, posing a fatal impact hazard.
• Recall 26489 — ZWILLING J.A. Henckels (Solingen, Germany) electric water kettles can have handles loosen and separate, spilling boiling contents and causing burns.
• Recall 26475 — Analemma water bottles imported by New Earth Technologies d.o.o. have an inner glass liner that can break, posing laceration and ingestion risks.

FDA — Drugs and Devices

No Class I actions in today's batch; all entries are Class II, firm-initiated voluntary recalls.

Sterility and contamination

• D-0518-2026 and D-0517-2026 — CareFusion 213 (El Paso, TX), a Becton Dickinson subsidiary, is recalling BD PurPrep povidone-iodine/isopropyl-alcohol antiseptic applicators (10.5 mL boxes of 25, and 26 mL cartons of 25 under NDC 54365-014-42) for lack of sterility assurance and potential contamination.
• D-0525-2026 — OASIS Medical (Glendora, CA) is recalling Oasis Tears PF preservative-free lubricant eye drops, 10 mL bottles (NDC 42126-6400-1), made in France by Excelvision, after FDA inspection observations raised sterility-assurance concerns.
• D-0527-2026 — Endo USA (Malvern, PA) is recalling Buprenorphine Hydrochloride Injection 0.3 mg/mL, 5×1 mL single-dose vials (NDC 42023-179-05) due to particulate matter identified as buprenorphine free base.
• D-0524-2026 — Central Admixture Pharmacy Services (CAPS) Los Angeles is recalling a patient-specific 1,660 mL TPN bag (Rx# 11-4909703-0-1) that was dispensed without insulin despite being listed on the label — an incorrect formulation defect.

Impurities, potency, and chemical contamination

• D-0514-2026 and D-0516-2026 — Ajanta Pharma (India), marketed by Ajanta Pharma USA (Bridgewater, NJ), is recalling Duloxetine Delayed-Release Capsules 30 mg (NDCs 27241-098-09, -03, -10) and 20 mg 60-count (NDC 27241-097-06) after 12- and 18-month stability testing showed N-nitroso-duloxetine impurity above FDA's 0.83 ppm limit.
• D-0523-2026 — Acella Pharmaceuticals (Alpharetta, GA) is recalling Naproxen Oral Suspension USP 125 mg/5 mL in 473 mL bottles (NDC 42192-619-16), made in Canada, for chemical contamination — lead and lithium above specification.
• D-0547-2026 — Ascend Laboratories (Parsippany, NJ) is recalling Metoprolol Succinate Extended-Release Tablets 25 mg (NDC 67877-590-01), manufactured by Alkem Laboratories in India, for failed dissolution specifications affecting drug release.
• D-0520-2026 — JB Chemicals/Unique Pharmaceutical Laboratories (Mumbai) Enalapril Maleate Tablets 20 mg, 1,000-count bottles distributed by Rising Pharma, are being recalled after an out-of-specification organic-impurities result.