Consumer Recalls Daily — 2026-07-10

TITLE: Recall Digest 2026-07-10: Gun safes, MagSafe chargers, and infant sleep products lead death-risk CPSC actions; Amgen and Camber flag foreign material in cardiac and seizure drugs

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CPSC — Consumer Products

Death-risk recalls lead the docket

• [26607] BBRKIN biometric gun safes sold exclusively on Amazon are recalled after the fingerprint locks were found to open for unauthorized users, an unusually severe firearm-access failure carrying explicit risk of death; consumers are told to disable the biometric feature and remove firearms immediately.
• [26610] Flaunt is recalling MagSafe-style lithium-ion power banks after reports the cells can overheat and ignite, posing fire and burn hazards with risk of death — the latest in a long run of pouch-cell recalls tied to portable phone chargers.
• [26608] Moodooy adult portable bed rails (sold on Amazon by Yuezhang) violate the mandatory ASTM standard: users can be entrapped between the rail and mattress, an asphyxiation pattern that has killed adults in prior recalls.
• [26609] WonderStone infant walkers (sold on Walmart.com by Wonder Stone Toys) fit through a standard doorway and fail the top-of-stairs stop test, in direct violation of 16 CFR 1216.
• [26582] Treatlife combination smoke/CO detectors sold on Amazon can fail to alarm during a fire — a rare and serious life-safety failure for a device whose entire purpose is alerting.

Infant sleep and child-hazard cluster

Several recalls this cycle target infant sleep and small-parts hazards, all citing risk of serious injury or death:

• [26596] AMASKY nursing pillows (sold on Amazon by Pretty-Life) violate both the nursing-pillow and infant-support-cushion standards; contours can obstruct an infant's airway.
• [26591] Vevor baby loungers violate the Safe Sleep for Babies Act's infant sleep-product rule — sides too low, foot openings too wide.
• [26594] POPOOO projecting LED finger-light toys and [26580] Honlyne LED party favors both fail button-cell battery accessibility requirements; [26600] Junpower CR2032 coin cells sold by JSNJ_Tech violate Reese's Law packaging and warning-label mandates; and [26578] Raychy children's light-up sneakers (imported by Carina and Rambo) have accessible coin cells.
• [26579] Small Fish Montessori busy-board toys can shed high-powered magnets — the classic multi-magnet intestinal-perforation hazard.
• [26598] Target's Gigglescape Under the Sea popping toy can shed its clear dome, releasing small balls (choking).
• [26593] Diamond Wipes International is recalling CVS Health medicated hemorrhoidal wipes because the lidocaine-containing packaging fails Poison Prevention Packaging Act child-resistance requirements.
• [26507] Kith Retail children's loungewear sets fail the mandatory children's sleepwear flammability standard (16 CFR 1615/1616).

Fire, burn, and appliance hazards

• [26606] Best Buy's Insignia gas ranges have front-mounted knobs that pets or passersby can bump on, igniting unattended fires — the same design defect that has driven multiple range recalls in recent years.
• [26611] Greenworks Tools is recalling 24V and 48V Kobalt yard power tools whose lithium-ion packs can short-circuit if charged via USB-C while still seated in the tool.
• [26595] Rowenta cordless vacuums and [26599] Cooper Lighting's Metalux Optimized High Bay LED fixtures both present overheating/fire hazards; the Metalux boards can contact the lens or nearby combustibles.
• [26581] Daikin Comfort Technologies is recalling Amana air conditioners and heat pumps because the heating element can remain energized during a ground fault even when switched off — a notable control-logic defect for HVAC gear.
• [26605] Conair's Cuisinart Propel+ Four Burner 3-in-1 gas grills have a tempered-glass pizza-oven window that can shatter in use (laceration).

Other notable actions

• [26601] Conair is separately recalling over one million Cuisinart grill brushes whose wire bristles can detach and lodge in food — an ingestion hazard that has historically caused ER visits and required surgical removal.
• [26592] Topyond pool drain ports and covers (sold by Jialyduu) violate the Virginia Graeme Baker Pool & Spa Safety Act's entrapment-protection standard.
• [26602] and [26603] Winco Fireworks International is recalling both its Unity 7 Shot 200-gram aerial cakes (tip-over) and Roman Candles 8 Shot units (shots blowing out sidewalls) — timely, given the recall dates just after the July 4 holiday.

FDA — Drugs and Devices

All FDA entries this cycle are Class II (temporary or medically reversible adverse consequences), but two clusters stand out.

Cross-contamination and foreign material in cardiac/CNS drugs

• [D-0626-2026] Annora Pharma (for Camber Pharmaceuticals) is recalling Lacosamide Tablets USP 100 mg, NDC 31722-813-60, after a complaint suggested a Selexipag 1000 mcg tablet (a pulmonary hypertension drug) was mixed into a bottle — a cross-contamination between two unrelated therapies dispensed to seizure patients.
• [D-0615-2026] and [D-0612-2026] Amgen is recalling Italian-manufactured Corlanor (ivabradine) 7.5 mg (NDC 55513-810-60) and 5 mg (NDCs 55513-800-99 and 55513-800-60) tablets for "presence of foreign substance" — two lots of the heart-failure drug in one week.
• [D-0617-2026] Direct Rx is recalling repackaged duloxetine DR 30 mg (Cymbalta; NDCs 61919-482-30 and 61919-482-60) for N-nitroso-duloxetine impurity above FDA's interim limit — the ongoing nitrosamine issue continues to surface in repackagers.

CGMP deviations and potency/formulation

• [D-0614-2026] Amgen's Sensipar (cinacalcet) 60 mg (NDC 55513-074-30) and [D-0611-2026] Ajanta's Fenofibrate Capsules USP 200 mg (NDC 27241-120-04) are both recalled for CGMP deviations.
• [D-0627-2026] Elevate Oral Care's Povi-One 10% povidone-iodine oral antiseptic (NDC 57511-0611-1) is subpotent.
• [D-0618-2026] Central Admixture Pharmacy Services recalled a patient-specific pediatric TPN bag (Rx# 24-1269856-0-1, 1295 mL) that was compounded without the labeled copper and famotidine — a compounding-pharmacy formulation error affecting a single pediatric patient but reportable given the vulnerable population.

Sterile device packaging

• [D-0622-2026] and [D-0623-2026] CareFusion 213 (a BD subsidiary) is recalling two configurations of BD ChloraPrep skin-prep applicators — the 1 mL Clear (NDC 54365-4…) and 1.5 mL FREPP Clear — for lack of assurance of sterility stemming from wrinkles in the paper lidding that may breach the seal. Hospitals should quarantine affected lots before pre-op use.