Consumer Recalls Daily — 2026-05-27

TITLE: Recall Digest 2026-05-27: Button-cell toys, Petzl harnesses, asbestos in squeeze toys; FDA pulls duloxetine, naproxen, BD PurPrep

---

CPSC: Consumer Products

The May 21 docket is dominated by deadly-hazard kids' product recalls, led by repeat button-cell offenders and an asbestos finding in a children's craft toy.

Children's products — death-risk hazards lead

• 26499 — The Orb Factory's *Orb Funkee* squeeze toys are being pulled after tremolite asbestos was detected in the kinetic sand fill, an inhalation-exposure hazard that escalates this well above the typical toy recall.
• 26497 and 26503 — ABC Trading is recalling two separate button-cell products (unspecified children's toys, and *WSDZ* light-up glasses) for violating the Reese's Law mandatory standard; battery compartments open without tools, posing a fatal ingestion hazard.
• 26483 — Missry Associates' *Misco Sports* Badminton Toy Sets join the button-cell pile-up: the shuttlecocks contain accessible coin cells, again in violation of the toy standard.
• 26484 (LiCB / Guangzhou Lichengbei) and 26465 (EEMB USA) — Loose lithium coin batteries sold on Amazon were packaged without the child-resistant blister packs and Reese's Law warning labels required by federal statute.
• 26502 — *PandaEar* portable hook-on chairs fail the mandatory standard because the crotch restraint can be removed without a tool, letting infants slip through; classified as a deadly fall hazard.
• 26493 and 26490 — Two kitchen-helper "tower stool" recalls landed the same day: *Cosyland* (Cosyland Official import) towers can collapse or allow torso entrapment, while *Guidecraft* towers have platforms that loosen over time and detach.
• 26481 — *Tiyol* pull-string teething toys (sold on Amazon by ZW Creations) have silicone strings longer than the standard permits, which can lodge in a child's throat — choking/respiratory hazard.
• 26477 — Allura Imports' youth bobcat-logo sweatshirts violate the children's upper-outerwear drawstring rule, a long-standing strangulation hazard category.

Powered equipment, vehicles, fall-protection

• 26482 — BRP is recalling *Can-Am* youth/adult ATVs because the Speed Limiter Mode can malfunction and cause unexpected acceleration; consumers are told to stop using the limiter immediately pending dealer remedy.
• 26501 — *Lil Pick Up* youth ATVs violate the federal ATV standard on multiple fronts: failed suspension requirements and a non-illuminating reverse indicator.
• 26494 — Generac Power Systems is expanding its prior recall of *Generac* and *DR Power* electric-start pressure washers to include additional models; the start/stop button can self-activate, creating a CO poisoning risk in enclosed spaces.
• 26488 — Petzl America's *ASTRO BOD FAST*, *ASTRO SIT FAST* and *CANYON GUIDE* harnesses can have the D-ring release, opening the attachment point — a fall fatality hazard for work-at-height professionals.
• 26487 — A second Petzl recall covers *SIMBA* and *SWAN EASYFIT* harnesses missing rivets in the FAST LT PIN-LOCK buckles, allowing the buckles to open under load.

Home, recreation, household goods

• 26504 — Bethlehem Lights' 10-inch illuminated ribbon spheres (sold by QVC) can overheat at the LEDs, a documented fire hazard tagged for serious injury or death.
• 26478 — *EVLWZL* and *Gunugu* mattresses fail the federal mattress flammability standard outright — a categorical fire-hazard pull.
• 26480 — Remy&shop / Shenzhen Jiangtou *Superbobi* pool drain covers violate the Virginia Graeme Baker Pool & Spa Safety Act entrapment requirements, posing drowning hazard to swimmers.
• 26485 — World Bright International's *Agio Menlo* woven patio swings, sold at Costco, can detach from the frame mid-use.
• 26479 — Minka Lighting Group's *Bardon* series pendant fixtures can have the frame separate from the downrod during installation, an overhead impact hazard.
• 26489 — ZWILLING J.A. Henckels (Solingen, Germany) is recalling electric water kettles whose handles can loosen and detach, spilling boiling water.
• 26475 — *Analemma* water bottles (New Earth Technologies d.o.o.) have inner glass liners that can shatter, creating laceration plus ingestion-of-glass risk.
• 26486 — Amazon's house-brand *Amazon Basics 55 lb. adjustable dumbbells* can shed weight plates mid-rep when the engagement mechanism fails — impact hazard.
• 26498 — HomeProGym resistance bands can separate from the handle under tension, snapping back at the user.

FDA: Drugs and Medical Devices

No Class I recalls today; the FDA docket is entirely Class II, but two themes stand out — nitrosamine impurities in generic SSRIs and sterility/contamination concerns at multiple finished-dosage facilities.

Impurities and contamination

• D-0514-2026 and D-0516-2026 — Ajanta Pharma Ltd. is recalling Duloxetine Delayed-Release Capsules in 30 mg (NDCs 27241-098-03/-09/-10) and 20 mg (NDC 27241-097-06) after 12- and 18-month stability testing showed N-nitroso-duloxetine above the FDA's 0.83 ppm limit — a continuing nitrosamine problem for the duloxetine class.
• D-0523-2026 — Acella Pharmaceuticals is pulling Naproxen Oral Suspension 125 mg/5 mL, 16 fl oz bottles (NDC 42192-619-16, made in Canada) for lead and lithium contamination above specification — notable because the suspension form is commonly pediatric/elderly use.
• D-0527-2026 — Endo USA is recalling Buprenorphine HCl Injection 0.3 mg/mL, 5×1 mL single-dose vials (NDC 42023-179-05) for visible particulate matter identified as buprenorphine free base.
• D-0547-2026 — Ascend Laboratories' Metoprolol Succinate ER Tablets 25 mg (NDC 67877-590-01, manufactured by Alkem Laboratories, India) failed dissolution specifications — a potency/release concern for a cardiovascular drug.
• D-0520-2026 — Rising Pharma / JB Chemicals (Unique Pharmaceutical Laboratories, Mumbai) is recalling Enalapril Maleate Tablets USP 20 mg in 1,000-count bottles for an out-of-spec organic impurities result.

Sterility and compounding errors

• D-0517-2026 and D-0518-2026 — CareFusion 213 (a Becton Dickinson subsidiary, El Paso) is recalling two configurations of *BD PurPrep* povidone-iodine/IPA skin prep applicators (NDC 54365-014-42 for the 26 mL carton) for potential contamination — a sterility-of-surgical-prep concern hospitals should action immediately.
• D-0525-2026 — Oasis Medical's *Oasis Tears PF* preservative-free lubricant eye drops, 10 mL (NDC 42126-6400-1, made in France at Excelvision), are being recalled out of caution after adverse FDA inspection observations at the contract manufacturer.
• D-0524-2026 — Central Admixture Pharmacy Services (CAPS) Los Angeles is recalling a patient-specific TPN bag (Rx# 11-4909703-0-1, 1,660 mL) that was compounded without the insulin listed on its label — a serious formulation error, though limited to a single patient-specific Rx.