Consumer Recalls Daily — 2026-04-28

TITLE: Recalls Daily — Infant loungers, tower stools and pressure washers dominate CPSC sweep; Fresenius Kabi saline pulled in broad sterility action

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CPSC — Consumer Products

The April 16 and April 23 recall waves are heavily weighted toward children's products, with multiple Class I-equivalent "risk of serious injury or death" notices. Lead items below cite explicit death/injury hazards.

Infant sleep and support products (suffocation/fall risk)

• HappyGira is recalling its Sweetie Baby and Style Life Eleven baby loungers for suffocation and fall hazards in violation of the federal Infant Sleep Products rule; consumers must destroy the loungers to obtain a full refund.
• Cpzzkq baby loungers, sold on Amazon by CetoPMax, are being pulled for failing the Infant Support Cushions standard; remedy requires removing the foam and pad before refund.
• ZOLIQUEX adult portable bed rails, sold on Amazon, violate the mandatory Adult Portable Bed Rails standard and pose entrapment and asphyxiation risk to vulnerable adults — full refund offered.

Children's tower stools — coordinated multi-importer recall

Three separate importers — AMZCMJ DGD (26433), TOETOL HOME (26432), and Wiifo (26430) — are recalling near-identical children's tower stools for entrapment and fall hazards carrying risk of serious injury or death. All three remedies require consumers to destroy the stool for a full refund, suggesting a shared OEM source.

Toys and children's products with ingestion/choking hazards

• Autobrush Sonic Pro children's toothbrush boxes (26434) violate the federal coin-battery standard, posing battery-ingestion death risk; Autobrush is offering a $5 refund after consumers remove the boxes from children.
• BlissfulDestiny magnetic stick figure sets sold on Walmart (26436) violate the toy magnet standard — magnet ingestion can cause fatal intestinal injury.
• JC Sales Lil' Buddies pet laser toys (26428) violate the button-cell battery standard, posing ingestion death risk to children handling the pet product.
• Choking/small-parts violations also drove recalls of KMUYSL Big Red Barn farm playsets (sold by MISSJUNE), ATOYUS activity cubes (sold by Melofaver US), and SpringFlower Montessori teething toy sets — all citing risk of serious injury or death.
• SEGMART mini round toddler trampolines (26414) carry a strangulation hazard from removable hammock, punching bag, hand ring and basketball-board accessories; remedy is accessory removal.
• Fun and Function is recalling children's metal multi-point swing frames (26413) for a fall hazard — full refund offered.
• Xingwenfeng's nvyue Magic Pocket Staffs (26409) pose projectile and laceration hazards.

Chemical and burn hazards

• mGanna sodium hydroxide pellet bags sold on Amazon by Archie Xpress (26429) violate child-resistant packaging requirements; the lye can cause severe chemical burns to skin and eyes.
• 32 Degrees heated socks (26435) are being recalled for a burn hazard, with returns through Costco for a full refund.
• Macy's is recalling Arch Studio tea kettles (26412) for a burn-hazard defect; refund issued by check.
• Fisher & Paykel (Thailand) free-standing professional gas ranges (26419) are recalled for a burn hazard in the oven section.

Electrical, fire and impact hazards

• Generac Power Systems is recalling portable generators (26407) for burn and fire hazards posing risk of serious injury or death; affected units can be checked at generac.com/about/recalls/GP-Carburetor.
• A coordinated pressure-washer recall hit three importers — Agiiman (26420), Fengrong Tool (26421) and Le Hao Tool (26422) — all for shock and electrocution hazards with risk of death; full refunds after destruction of the unit.
• Apex Gaming PCs is recalling Manik- and Apex-branded ATX computer power supplies (26426) for electrical shock and electrocution risk; remedy is a free repair.
• Tzumi Electronics is recalling FitRx SmartBell quick-select adjustable dumbbells (26431) after reports of impact-hazard injuries; free replacement of dumbbell and tray offered.

FDA — Drugs

All ten FDA actions this cycle are Class II (temporary or medically reversible adverse health consequences), firm-initiated voluntary recalls. No Class I drug or device recalls in this batch.

Fresenius Kabi sodium chloride sterility sweep (March 11)

Fresenius Kabi USA has voluntarily recalled six sodium chloride injection presentations for lack of assurance of sterility — a significant action for a hospital staple. Affected lots span:

• D-0427-2026: 0.9% NaCl 2,250 mg/250 mL freeflex bag, NDC 65219-470-05.
• D-0424-2026: 0.45% NaCl 1.125 g/250 mL freeflex bag, NDC 63323-626-03.
• D-0432-2026: 0.9% NaCl 900 mg/100 mL, 500 mL single-dose freeflex bag, NDC 65219-432-20.
• D-0426-2026: 0.9% NaCl 100 mL freeflex bag, NDC 65219-468-05.
• D-0428-2026: 0.9% NaCl 4,500 mg/500 mL freeflex bag, NDC 65219-472-05.
• D-0430-2026: 0.9% NaCl 100 mL single-dose freeflex bag distributed by BD (Becton Dickinson), manufactured by Fresenius Kabi.

Hospital pharmacy buyers should audit inventory across all listed NDCs given the breadth of the action.

Fagron compounded vancomycin (March 20)

Fagron Sterile Services (Wichita, KS) is recalling two compounded vancomycin HCl IV bag presentations for lack of sterility assurance compounded with a defect in which a blue break-off part could detach from the administration port:

• D-0440-2026: Vancomycin HCl 1.25 g in 250 mL 0.9% NaCl, NDC 71266-5083-01.
• D-0441-2026: Vancomycin HCl 1.5 g in 250 mL 0.9% NaCl, NDC 71266-5085-01.

Teva/Actavis clonidine patches (March 19)

Teva Pharmaceuticals USA is recalling two strengths of Clonidine Transdermal System manufactured by Actavis Laboratories UT for CGMP deviations involving use of an unapproved raw material — D-0472-2026 (0.1 mg/day) and D-0473-2026 (0.2 mg/day), each supplied in 4-system cartons. Prescribers managing hypertensive patients on patch therapy should verify lot status with distributors.