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Kori Gey Water Elf craft toy kits sold on Amazon contain a LED light with a button cell battery that children can easily access and open. Swallowed button batteries can cause serious internal injuries, chemical burns, and death.

Serious·CPSC·Jan 8, 2026

The Lterfear Multifunction Pounding Game (model D888) contains high-powered magnets that can detach and be swallowed by children. When multiple magnets are ingested, they can attract each other inside the digestive system, causing serious internal injuries including intestinal perforation, blockage, and potentially death.

Serious·CPSC·Jan 8, 2026

Yolaah bed rails (model BR-01) can trap users between the rail and mattress, creating a serious risk of injury or death by asphyxiation. The rails also lack required warning labels. About 14,250 units were sold online through Amazon between September and October 2025.

Serious·CPSC·Jan 8, 2026·Yolaah

Vasicar 18-drawer dressers can tip over and trap children if not securely anchored to a wall. These dressers do not meet federal safety standards for furniture stability. About 4,155 units were sold online between September and November 2025.

Serious·CPSC·Jan 8, 2026

Sangohe adult portable bed rails can trap users between the rail and mattress, creating a serious risk of injury or death by asphyxiation. The rails also lack required warning labels. About 26,200 units sold online at Amazon and Walmart between August 2023 and October 2025 are affected.

Serious·CPSC·Jan 8, 2026·Sangohe

Rattan 6-Drawer Dressers (model YD001) sold on Amazon can tip over and trap children if they are not securely anchored to a wall. The dressers do not meet federal safety standards for furniture stability. About 870 units were sold between September and November 2025.

Serious·CPSC·Jan 8, 2026

NFSVLB baby bath seats (model ZY2025) can tip over during use and have openings that allow infants to slip down and become trapped underwater. The seats do not meet safety standards for infant bath products. About 1,430 seats were sold on Amazon between May and October 2025.

Serious·CPSC·Jan 8, 2026

Marcus Adler Glove Co. is recalling Julie and Judah brand pajama pants and shorts because they don't meet federal flammability standards for children's sleepwear. These garments could catch fire more easily than safe sleepwear, risking burn injuries to children.

Serious·CPSC·Jan 8, 2026

Kalencom recalled SARO Braided Crib Bumpers (Model 1374) because they violate the federal ban on crib bumpers and can block an infant's breathing, creating a suffocation risk. The bumpers were sold in salmon, gray, and mint colors at MacroBaby, Kalencombaby.com, and Target.com from May 2024 through October 2025. No injuries have been reported.

Serious·CPSC·Jan 8, 2026·Kalencom

BabyBond retractable safety gates can allow a child's torso to fit through the gap between the gate and floor, creating a serious entrapment risk. The gates were sold at Target.com between November 2024 and October 2025. No injuries have been reported, but the hazard poses a risk of serious injury or death.

Serious·CPSC·Jan 8, 2026·BabyBond

Pieces inside DR Power leaf vacuums can come loose or debris can pierce the chute, causing material to shoot out and potentially cut users or bystanders. The company has received 46 reports of debris being ejected, though no injuries have been reported yet.

Serious·CPSC·Jan 8, 2026

Agrish adult portable bed rails (models 2512, 2513, and 2516) can trap users between the rail and mattress, creating a serious risk of entrapment and suffocation. The rails do not meet federal safety standards. About 5,000 units were sold on Amazon between April and October 2025.

Serious·CPSC·Jan 8, 2026·Lebo

Diasol has recalled specific lots of its liquid concentrate used in bicarbonate dialysis machines. The FDA determined that the safety and efficacy of this product cannot be assured. The recall affects 7,200 gallons distributed across six states.

Serious·FDA·Dec 31, 2025·Diasol6 products

Zimmer, Inc. recalled certain Affixus 9 mm femoral nails (model 815509360, length 360 mm) because the shaft may be undersized and prone to breaking. If the implant fractures, it could cause pain, improper bone healing, tissue damage, or require additional surgery.

Serious·FDA·Dec 31, 202517 products

Alcon Custom Pak sterile surgical procedure packs used in eye surgery may have incomplete seals that could compromise sterility. This affects 151 units across specific lot numbers. No injuries have been reported.

Serious·FDA·Dec 31, 2025

Draeger, Inc. is recalling certain Vapor 2000 anesthetic vaporizers because an internal component was manufactured with impurities and did not meet quality specifications. The affected units are identified by specific serial numbers and were distributed worldwide, including across the United States.

Serious·FDA·Dec 31, 20252 products

Carousel Candies is recalling two 5 oz. Choceur holiday bark products sold in standup pouch bags: Choceur Pecan Cranberry & Cinnamon Holiday Bark and Choceur Cookie Butter Holiday Bark. The bags were sold nationwide at Aldi stores, and wheat is not listed on the label. No injuries have been reported.

Serious·FDA·Dec 31, 20252 products

Wegmans Deluxe Mixed Nuts in two sizes may be contaminated with Salmonella, a bacteria that can cause serious illness. The affected products were distributed to stores in Pennsylvania and New York. No illnesses have been reported yet.

Serious·FDA·Dec 31, 2025

First & Last Tavern is recalling three pasta sauces because they may be contaminated with Clostridium botulinum, the bacteria that causes botulism. The products are Traditional (meat flavored), Marinara (tomato & basil) and Puttanesca (olives, capers, hot peppers), all 26 fl oz jars, and they were distributed in Connecticut and Massachusetts. No illnesses have been reported.

Serious·FDA·Dec 31, 2025·First & Last Tavern3 products

Wegmans grated Pecorino Romano cheese (Locatelli brand, item #270010) sold in clear plastic tubs may be contaminated with Listeria monocytogenes, a bacteria that can cause serious illness. The affected cheese was sold between November 29 and December 7, 2025, in Wegmans stores across the Northeast and Mid-Atlantic regions.

Serious·FDA·Dec 31, 2025

Publix Raspberry Coffee Cake (15 oz.) was mislabeled—the product actually contains Maple Walnut Coffee Cake, but walnuts were not listed on the package label. People with walnut allergies could have a serious reaction if they eat this product.

Serious·FDA·Dec 31, 2025

Mountain West Food Group is recalling approximately 2,855 pounds of Forward Farms grass-fed ground beef due to possible E. coli O26 contamination. The contamination was discovered during routine testing. No illnesses have been reported so far.

Serious·USDA·Dec 27, 2025

Abbott Laboratories is recalling certain Alinity ci-series System Control Modules with software version 3.6.1 or lower due to a performance issue that could produce inaccurate lab test results. The issue affects multiple analytes and was discovered during Abbott's internal testing.

Serious·FDA·Dec 24, 2025

A speaker component change in certain PATH Madsen Accuscreen DPOAE probes can cause technical distortions that mimic real hearing responses. This may result in incorrect "PASS" outcomes on infant hearing screening tests when a baby should have failed. The issue occurs when high stimulus levels combine with the device's sensitivity settings.

Serious·FDA·Dec 24, 2025·PATH

Fresenius Medical Care identified several software problems in the 5008X CAREsystem +CLiC +CDX dialysis machine that could interfere with patient treatment. One anomaly could potentially cause the machine to stop treatment if certain conditions occur. This affects 115 units with software versions older than 4.82.4.

Serious·FDA·Dec 24, 2025

GE Healthcare is recalling certain Carestation 600 and 700 Series anesthesia systems, along with a related power management board part, because they may unexpectedly shut down if AC power is unplugged or lost. These systems have no continuous backup power and do not automatically switch to battery, so they reboot and may briefly interrupt ventilation and anesthetic delivery without returning to previous settings. The recall covers 3 product entries with about 2,368 units affected, and no injuries have been reported.

Serious·FDA·Dec 24, 20253 products

Fresenius Kabi has recalled software version 5.10.1 and earlier for the Ivenix Infusion System due to anomalies that could cause serious patient harm. The affected software is used to control the delivery of fluids to patients in medical settings. About 30 units have been distributed across multiple U.S. states.

Serious·FDA·Dec 24, 2025

The Whole Herb Company is recalling senna leaves (Item No. SEN15001, Lot No. 003279ST) because they may be contaminated with Salmonella. The recall affects approximately 3,580 pounds of product distributed in California, New Jersey, and Canada.

Serious·FDA·Dec 24, 2025

Mamtakim is recalling two Belevini dried salted whole smelt products, KORUSHKA and BICHKI, each sold in 5.29 oz vacuum packs. The fish may be contaminated with Clostridium botulinum, the bacterium that causes botulism, because the fish were not eviscerated (cleaned). The products were distributed in NY, TX, PA, NJ and FL, and no illnesses have been reported.

Serious·FDA·Dec 24, 2025·Belevini2 products

Food to Live brand Organic Supergreens Powder Mix has been recalled because it may be contaminated with Salmonella, a bacteria that can cause serious illness. The affected product comes in multiple sizes (8 oz to 12 lb) with lot codes between SO-69006 and SO-72558.

Serious·FDA·Dec 24, 20252 products