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Consumer Recalls Daily2026-05-18May 18, 2026

Consumer Recalls Daily — 2026-05-18

TITLE: Recalls Daily — Injury-and-death hazards dominate CPSC week; FDA flags Wells Pharma fentanyl, sterile eye drops

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CPSC — Consumer Products

Of the 25 CPSC notices in the two-week window, the overwhelming majority cite "risk of serious injury or death" language, with hazards concentrated in three buckets: fall/impact, child ingestion, and flammability/CO. No fatalities are reported in the underlying notices, but several products are pulled for violating mandatory federal standards.

Lead: Crash, fall and CO hazards with injury-or-death language

  • [26482] BRP is recalling Can-Am ATVs after the speed limiter control was found to malfunction and cause unexpected acceleration, a crash hazard CPSC flags with explicit risk of death; owners are told to stop using Speed Limiter Mode immediately.
  • [26494] Generac Power Systems (Waukesha, WI) is expanding its electric-start pressure washer recall to additional Generac and DR Power models after the start/stop button can self-activate, posing a carbon-monoxide death risk in enclosed spaces.
  • [26487] and [26488] Petzl America is recalling two harness lines — SIMBA and SWAN EASYFIT (missing rivets in the FAST LT PIN-LOCK buckles) and the ASTRO BOD FAST, ASTRO SIT FAST and CANYON GUIDE harnesses (D-ring can release) — both posing fall hazards to climbers and work-at-height professionals.
  • [26479] Minka Lighting's Bardon Series pendant fixtures can detach from the downrod during installation, an impact hazard CPSC describes as carrying risk of serious injury or death.
  • [26485] World Bright International's Agio Menlo woven patio swings, sold at Costco, can have the seat detach from the frame mid-use, a fall hazard.

Children's products — the bulk of this week's docket

  • [26493] Cosyland children's tower stools (imported by Cosyland Official) can collapse, tip, or trap a child's torso through front/back openings — a triple tip-over, fall and entrapment hazard. [26490] Guidecraft's children's standing towers were separately recalled the same day after the inside platform can loosen and detach.
  • [26448] UHOMEPRO 5-drawer dressers violate the federal mandatory standard for clothing storage units (STURDY Act) and are unstable when unanchored, with tip-over and entrapment risk to children.
  • [26468] Svnntaa adult portable bed rails (sold on Amazon by Eokeanon) violate the mandatory bed-rail standard, with users at risk of entrapment and asphyxiation between rail and mattress.
  • [26477] Allura Imports youth bobcat-logo sweatshirts contain drawstrings that violate federal children's upper-outerwear rules, a strangulation hazard.
  • Three separate helmet recalls fail the mandatory bicycle-helmet standard for positional stability and certification: [26467] Favoto bicycle helmets (Amazon) and [26470] multi-purpose helmets sold on Temu by Foubeaka and Geniuss.
  • Choking and respiratory hazards: [26481] Tiyol pull-string teething toys (sold on Amazon by ZW Creations) have non-compliant silicone strings that can lodge in the throat; [26472] Rainbow Wall xylophone toys (Amazon, Justforjoyful) have a drumstick with a spherical end that fails the toy standard.

Button-cell and coin-battery ingestion — a Reese's Law cluster

CPSC issued four related actions targeting button/coin-cell access in violation of either Reese's Law packaging requirements or the toy standard:

  • [26484] LiCB (Guangzhou Lichengbei Battery Technology), sold via Amazon, shipped lithium coin batteries without child-resistant packaging or Reese's Law warning labels.
  • [26465] EEMB USA recalled battery pouches for the same Reese's Law packaging failure.
  • [26483] Missry Associates' Misco Sports badminton toy sets and [26466] ZMC Group's multiple light-up toys both violate the mandatory toy standard because button cells are accessible to children.

Other notable consumer goods

  • [26486] Amazon is recalling its Amazon Basics 55-lb adjustable dumbbells after weight plates can fail to engage and dislodge mid-lift — an impact hazard.
  • [26489] ZWILLING J.A. Henckels (Solingen, Germany) electric water kettles can have the handle separate from the body, spilling boiling water — a burn hazard.
  • [26480] Superbobi pool drain covers (manufactured by Shenzhen Jiangtou Technology / Remy&shop) violate the Virginia Graeme Baker Pool & Spa Safety Act, posing entrapment and drowning hazards.
  • [26475] Analemma water bottles (imported by New Earth Technologies d.o.o.) have an inner glass liner that can shatter, posing laceration and ingestion hazards.
  • [26478] EVLWZL and Gunugu mattresses fail the federal mattress flammability standard outright — a fire-injury-or-death recall.
  • [26469] Natural Pigments LLC (Willits, CA) recalled Rublev Colours gum turpentine and mineral spirits bottles for violating the Poison Prevention Packaging Act's child-resistant packaging rule.

FDA — Drugs

All ten FDA entries this cycle are Class II, firm-initiated voluntary recalls. Two clusters dominate.

Wells Pharma of Houston — five-product cGMP recall

Wells Pharma of Houston LLC initiated voluntary recalls on 2026-04-01 of multiple controlled-substance injectables for unspecified cGMP deviations:

  • [D-0503-2026] fentaNYL Citrate Injectable Solution, 1000 mcg/100 mL, NDC 73702-202-02; [D-0504-2026] fentaNYL Citrate in 0.9% NaCl, 2500 mcg/250 mL, NDC 73702-202-03; [D-0505-2026] fentaNYL Citrate, 1250 mcg/25 mL, NDC 73702-204-25; [D-0506-2026] fentaNYL Citrate in 0.9% NaCl, 1000 mcg/50 mL, NDC 73702-203-65; and [D-0507-2026] Ketamine HCl Injectable, 50 mg/mL, NDC 73702-302-31. The five-NDC sweep suggests a facility-wide finding rather than a single-lot failure.

Sterile ophthalmic drops — four recalls tied to FDA inspections

Four lubricant eye-drop products were pulled in April for "lack of assurance of sterility" following FDA inspection observations at manufacturing sites:

  • Thea Pharma, Inc. (Waltham, MA) — [D-0500-2026] iVIZIA Sterile Lubricant Eye Drops, Povidone 0.5%, NDC 82584-700-11, and [D-0501-2026] the Similasan-branded iVIZIA equivalent, NDC 59262-700-11, both Made in France.
  • [D-0492-2026] Alcon Research LLC — GenTeal Tears Lubricant Eye Gel 10g, NDC 0065-8064-01, distributed by Alcon Laboratories (Fort Worth, TX).
  • [D-0499-2026] Scope Health — Optase Dry Eye Intense Drops (Glycerin 0.2%), NDC 72972-002-01.

Other

  • [D-0526-2026] Hikma Pharmaceuticals USA (Berkeley Heights, NJ) recalled Alendronate Sodium Oral Solution 70 mg/75 mL, NDC 0054-0282-59, after out-of-specification assay results in bottles that had been stored on their side — a stability/packaging-orientation issue worth noting for pharmacies.

No Class I drug recalls, device recalls, or food/cosmetic recalls appear in today's FDA feed.