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Consumer Recalls Daily2026-05-19May 19, 2026

Consumer Recalls Daily — 2026-05-19

TITLE: Recalls Daily — Can-Am ATVs, Petzl harnesses, Generac washers lead injury-risk wave; Wells Pharma fentanyl line-wide pull

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CPSC — Consumer Products

Lead: Recalls citing serious injury or death risk

  • BRP Can-Am ATVs (#26482) are being recalled because the speed limiter control can malfunction and cause unintended acceleration; BRP is telling owners to stop using Speed Limiter Mode immediately pending a fix. Class I-equivalent hazard with explicit death risk cited.
  • Generac and DR Power electric-start pressure washers (#26494) — Generac Power Systems of Waukesha, WI is expanding an earlier recall to additional models after reports the electronic start/stop button can self-activate, posing a carbon monoxide poisoning death risk if the unit runs in an enclosed space.
  • Petzl America issued two simultaneous fall-hazard recalls: the ASTRO BOD FAST, ASTRO SIT FAST and CANYON GUIDE harnesses (#26488) can have a D-ring that releases, opening the attachment point, and the SIMBA and SWAN EASYFIT harnesses (#26487) are missing rivets in the FAST LT PIN-LOCK buckles, which can open under load. Work-at-height professionals are told to stop use immediately.
  • Minka Lighting Group's Bardon Series pendant fixtures (#26479) can detach from the downrod during installation, posing an impact hazard serious enough to warrant a death-risk citation.
  • Agio Menlo woven patio swings (#26485), imported by World Bright International and sold at Costco, can have the seat detach from the frame mid-use — a fall hazard with injury/death risk.
  • Analemma water bottles (#26475), imported by New Earth Technologies d.o.o., can have the inner glass liner shatter, creating laceration and ingestion hazards.
  • ZWILLING J.A. Henckels electric water kettles (#26489), from the German parent firm in Solingen, can have the handle loosen and separate, spilling boiling water — a serious burn hazard.
  • Amazon Basics 55-lb. adjustable dumbbells (#26486) can dislodge weight plates during adjustment; Amazon is running the recall directly and telling consumers to stop use.

Children's products — high concentration this cycle

  • Cosyland children's tower stools (#26493) can collapse or tip and have torso-sized openings, triggering combined tip-over, fall, and entrapment death-risk citations; imported by Cosyland Official.
  • Guidecraft children's standing towers (#26490) have a platform that can loosen or detach over time, posing a fall hazard to toddlers.
  • UHOMEPRO 5-drawer dressers (#26448) violate the mandatory clothing-storage-unit stability standard, with tip-over and entrapment death-risk citations.
  • Svnntaa adult portable bed rails (#26468), sold on Amazon by Eokeanon, violate the mandatory standard for adult bed rails with entrapment and asphyxiation risk.
  • Allura Imports youth bobcat-logo sweatshirts (#26477) have prohibited drawstrings in violation of federal children's outerwear rules — a strangulation hazard.
  • Tiyol pull-string teething toys (#26481), sold on Amazon by ZW Creations, have silicone strings longer than allowed that can reach the back of the throat.
  • Rainbow Wall toys (#26472) from Justforjoyful on Amazon have a xylophone drumstick with a spherical end that fails the small-parts standard.

Three separate button-cell battery ingestion actions ran this cycle: LiCB lithium coin batteries (#26484) from Guangzhou Lichengbei, sold on Amazon, lack the Reese's Law–required child-resistant packaging; EEMB USA battery pouches (#26465) are similarly non-compliant; and Missry Associates Misco Sports badminton sets (#26483) and ZMC Group light-up toys (#26466) both contain accessible button cells in violation of the children's toy standard.

Other notable CPSC actions

  • Favoto bicycle helmets (#26467) (sold on Amazon) and Foubeaka/Geniuss multi-purpose helmets (#26470) (sold on Temu) both fail positional-stability and certification requirements under the mandatory bicycle helmet standard.
  • Superbobi pool drain covers (#26480), manufactured by Shenzhen Jiangtou Technology dba Remy&shop, violate the Virginia Graeme Baker Pool & Spa Safety Act — entrapment/drowning hazard.
  • EVLWZL and Gunugu mattresses (#26478) fail the mandatory mattress flammability standard.
  • Natural Pigments Rublev Colours gum turpentine and mineral spirits (#26469), of Willits, CA, were sold without the Poison Prevention Packaging Act–required child-resistant closures.

FDA — Drugs

Lead

No Class I drug recalls were posted in this batch; all ten entries are Class II. The dominant story is a line-wide Wells Pharma of Houston pull.

  • Wells Pharma of Houston LLC (5265 Kitty Drive, Houston, TX 77054) is recalling its compounded ketamine HCl injection 50 mg/mL (NDC 73702-302-31, #D-0507-2026) alongside four fentanyl citrate injectable solution presentations — 1000 mcg/50 mL in 0.9% NaCl (NDC 73702-203-65, #D-0506-2026), 2500 mcg/250 mL (NDC 73702-202-03, #D-0504-2026), 1000 mcg/100 mL (NDC 73702-202-02, #D-0503-2026), and 1250 mcg/25 mL (NDC 73702-204-25, #D-0505-2026) — all firm-initiated on 2026-04-01 over cGMP deviations. Hospital pharmacies stocking compounded narcotics from Wells Pharma should expect to quarantine across the catalog.

Sterility cluster — ophthalmics

A second clear pattern: four separate sterile eye-product recalls driven by FDA inspection findings.

  • Thea Pharma Inc. (Waltham, MA) pulled two SKUs of iVIZIA Sterile Lubricant Eye Drops (Povidone 0.5%), 10 mL — co-branded Similasan/iVIZIA (NDC 59262-700-11, #D-0501-2026) and the standalone iVIZIA (NDC 82584-700-11, #D-0500-2026) — both made in France and recalled 2026-04-23 for lack of sterility assurance tied to cGMP deviations at the manufacturer.
  • Alcon Research LLC recalled GenTeal Tears Lubricant Eye Gel, 10 g (NDC 0065-8064-01, #D-0492-2026) on 2026-04-21 over FDA inspection observations.
  • Scope Health recalled Optase Dry Eye Intense Drops (Glycerin 0.2%), 0.33 fl oz (NDC 72972-002-01, #D-0499-2026) for the same sterility-assurance reason on 2026-04-20.

Other

  • Hikma Pharmaceuticals USA (#D-0526-2026) recalled Alendronate Sodium Oral Solution 70 mg/75 mL, 4×75 mL single-dose bottles (NDC 0054-0282-59) on 2026-04-07 after out-of-specification assay results in bottles that had been stored on their side — a storage-orientation-sensitive failure pharmacists should flag.