Consumer Recalls Daily — 2026-04-25

TITLE: Recalls Daily — Children's tower stools, baby loungers lead death-risk CPSC sweep; Fresenius Kabi saline pulled across nine NDCs

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CPSC — Consumer Products

Death-risk hazards: nursery and child products dominate

The week's most severe CPSC actions cluster around infant and toddler gear, with multiple firms cited for violating mandatory federal safety standards.

• Three importers — AMZCMJ DGD (26433), TOETOL HOME (26432), and Wiifo (26430) — recalled children's tower stools that can collapse or tip, with side openings large enough for a child's torso to pass through, posing entrapment, fall, and death hazards.
• Autobrush (26434) recalled its Sonic Pro Children's Toothbrush delivery boxes for violating the federal coin-battery standard; the lithium cell is accessible to children, posing fatal ingestion risk.
• Two baby lounger actions hit Amazon sellers: Cpzzkq loungers (26438) sold by CetoPMax violate the infant support cushion standard (suffocation), and HappyGira's Sweetie Baby and Style Life Eleven loungers (26437) violate the infant sleep products standard with sub-minimum side heights.
• SEGMART (26414) mini round toddler trampolines were recalled because hammock, punching-bag, and hand-ring straps can entangle young children, posing strangulation and death hazards.
• ZOLIQUEX (26425) adult portable bed rails sold on Amazon violate the mandatory adult bed-rail standard, posing entrapment and asphyxiation risk between rail and mattress.

Choking, magnet, and battery ingestion hazards

• MISSJUNE's KMUYSL Big Red Barn farm animal playsets (26440) and Melofaver US's ATOYUS activity cubes (26411) were pulled on Amazon for violating the small-parts ban — detachable fence handles and xylophone screws/clock hands on toys marketed to under-threes.
• BlissfulDestiny (26436) magnetic stick figure sets sold on Walmart contain loose high-powered magnets that can attract through intestinal tissue if swallowed, violating the mandatory toy standard.
• SpringFlower's Montessori toy sets (26427) were recalled for an airplane-shaped teething toy with tentacle ends that violate the teething-toy provision of the toy standard.
• JC Sales' Lil' Buddies Pet Laser Toys (26428) were recalled for accessible button-cell batteries in violation of Reese's Law packaging requirements.

Burn, shock, and impact hazards on appliances and tools

• Generac Power Systems (26407) recalled portable generators after determining gasoline can leak from the carburetor on first fill, posing fire and burn risk — death hazard noted.
• Fisher & Paykel (26419) free-standing professional gas ranges, manufactured in Thailand, can experience delayed ignition that causes gas accumulation and the oven door to blow open from combustion.
• Three Chinese pressure-washer brands — Agiiman (26420), Fengrong Tool (26421), and Le Hao Tool (26422) — were pulled for lacking integral GFCI protection, posing shock and electrocution risk.
• Apex Gaming PCs (26426) recalled Manik- and Apex-branded ATX power supplies for missing the permanent on-product electrical-hazard warning label.
• Tzumi Electronics' FitRx SmartBell Quick-Select adjustable dumbbells (26431) can shed weight plates from the handle mid-lift, an impact hazard.
• Macy's (26412) recalled Arch Studio tea kettles whose handles detach when heated; 32 Degrees (26435) recalled heated socks that can burn wearers during high-intensity activity from combined heat, friction, moisture, and pressure.

Other notable actions

• Fun and Function (26413) recalled children's metal multi-point swing frames that can crack mid-use, a fall hazard.
• Archie Xpress (26429) sold mGanna sodium hydroxide (lye) pellet bags on Amazon without child-resistant packaging required by the Poison Prevention Packaging Act, posing chemical-burn risk.
• Xingwenfeng's nvyue Magic Pocket Staffs (26409) were recalled because the protective pin can fail and the staff expands too rapidly to react to, a projectile and laceration hazard.

FDA — Drugs

Class II: Fresenius Kabi saline pulled across the line

Fresenius Kabi USA (Lake Zurich, IL) initiated a sweeping voluntary Class II recall on 2026-03-11 covering at least seven freeflex-bag saline presentations for "Lack of Assurance of Sterility." The affected lots span 0.9% Sodium Chloride Injection in 100 mL (NDC 65219-468-05, D-0426-2026), 250 mL (NDC 65219-470-05, D-0427-2026), and 500 mL (NDC 65219-472-05, D-0428-2026) freeflex bags; 0.45% Sodium Chloride Injection 250 mL (NDC 63323-626-03, D-0424-2026); a 500 mL Single Dose presentation (NDC 65219-432-20, D-0432-2026); and 100 mL Single Dose bags distributed by BD (D-0430-2026). Hospitals carrying any of these NDCs should pull stock and check lot/expiry against the firm's notice.

Class II: Compounded vancomycin and clonidine patches

• Fagron Sterile Services (Wichita, KS) recalled compounded Vancomycin HCl 1.25 g/250 mL (NDC 71266-5083-01, D-0440-2026) and 1.5 g/250 mL (NDC 71266-5085-01, D-0441-2026) preparations on 2026-03-20, citing both lack of sterility assurance and a defect in which the blue Break-Off-Part can detach from the administration port — a delivery-integrity issue on top of the sterility concern.
• Teva Pharmaceuticals USA recalled two strengths of Clonidine Transdermal System manufactured by Actavis Laboratories UT — 0.1 mg/day (D-0472-2026) and 0.2 mg/day (D-0473-2026) — on 2026-03-19 for CGMP deviations involving an unapproved raw material in the patches.

No Class I drug recalls and no death-citing FDA actions appear in today's feed.