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DJO is recalling four DONJOY IceMan cold therapy unit models, about 2,584 units in total, because a connector can break. A broken connector may temporarily interrupt prescribed cold therapy. No injuries have been reported, and the units were sold in the U.S. and Canada.

Moderate·FDA·May 20, 2026·DJO4 products

Fun and Function's metal multi-point swing frames (model MW7661) can crack or break during use, causing children to fall. The company has received 10 reports of frames cracking or breaking, with two children sustaining bruises.

Moderate·CPSC·Apr 16, 2026

Morovan gel nail polish remover (15ml bottle, turquoise with white cap) was found to contain methylene chloride and chloroform—chemicals prohibited in cosmetics. Methylene chloride may cause cancer and is not allowed in cosmetics at any level under FDA regulations. About 4,000 units were sold on Amazon between August 2025 and January 2026.

Moderate·FDA·Apr 9, 2026

Head USA ski boots from 2015–2022 with fluorescent yellow shells or soles can deteriorate and break during use, creating a serious fall risk. The company has identified specific model numbers and article codes affected by this defect. No injuries have been reported, but the boots pose a hazard if worn.

Moderate·CPSC·Apr 9, 2026

Blaine Labs is recalling three lot numbers of Revitaderm and Tridergel wound care gel (1 oz. and 3 oz. bottles/tubes) because they may contain Lysinibacillus fusiformis, a bacterium found in the environment. The affected products were distributed to healthcare providers only, not sold in stores. No injuries have been reported so far.

Moderate·FDA·Apr 8, 2026·Blaine Labs

K.C. Pharmaceuticals issued a recall of sterile eye drops sold under multiple brand names (including Walgreens, Good Sense, Kroger, CVS, and others) because the manufacturer cannot confirm the products remain sterile. The affected bottles were distributed nationwide. No injuries have been reported.

Moderate·FDA·Apr 8, 20268 products

The USDA retracted a public health alert issued on April 1, 2026, for Walmart Great Value Fully Cooked Dino Shaped Chicken Breast Nuggets with a "Best If Used By" date of February 10, 2027. The initial alert was based on a laboratory test that showed elevated trace levels of lead, but follow-up testing found no lead contamination in the product. The USDA determined the original test result was a false positive caused by contamination in the laboratory during analysis, not in the food itself.

Moderate·USDA·Apr 6, 2026

Waldemar Link is recalling two Embrace Drill Tower instruments used in shoulder surgery, 149 units in total. The surgical technique's overview lists some article numbers incorrectly, though the individual surgical steps in the technique are correct. No injuries have been reported.

Moderate·FDA·Apr 1, 20262 products

Elekta has recalled certain Leksell Gamma Knife Perfexion and Icon radiosurgery systems because an adapter component may not be properly aligned or locked in place. This could affect the accuracy of radiation delivery during treatment. No injuries have been reported.

Moderate·FDA·Mar 25, 2026

Some Stryker Cub Pediatric Cribs sold in the USA are missing two warning labels on the access doors. This affects 590 cribs with specific serial numbers. No injuries have been reported.

Moderate·FDA·Mar 25, 2026

Wawa Beverage Company discovered plastic material on the fill line of some 16 oz bottles of chocolate low-fat milk. The affected milk was distributed in New Jersey, Maryland, Delaware, and Pennsylvania. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·Wawa4 products

Strides Pharma Children's Ibuprofen Oral Suspension (100 mg per 5 mL) has been recalled because some bottles contain gel-like masses and black particles. The affected bottles are 4 FL OZ (120 mL) size with lot numbers 7261973A or 7261974A, expiring 01/31/2027. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·Strides

Physio-Control infant and child defibrillator electrodes may separate or peel apart during use, which could prevent proper delivery of therapy. The affected electrodes are pre-gelled, self-adhesive pads designed for use with automated external defibrillators (AEDs) on children under 8 years old or weighing less than 55 pounds. No injuries have been reported.

Moderate·FDA·Mar 18, 2026·Physio-Control

The rivets that hold up the swing seat in certain LFTE USA playground swings can fail without warning, causing the seat to fall and potentially injure children. The company has received one report of a child falling from a broken swing. Only swings with model number 999604 and marked with code "LF-65708" are affected.

Moderate·CPSC·Mar 12, 2026

Olympus has identified a mis-wired component in certain ShockPulse-SE Lithotripsy System generators (model SPL-G) that can cause electrical noise in the ultrasonic circuit. This noise may reduce the system's reliability and delay treatment. The recall affects 55 units distributed internationally.

Moderate·FDA·Mar 11, 2026

Tippy Toes apple pear banana baby food pouches may contain patulin, a naturally occurring toxin found in apples. The affected product is lot 07174 with a best-by date of 07/17/2026. No illnesses have been reported.

Moderate·FDA·Mar 11, 2026·IF Holding II

ACME United Corporation is recalling multiple lots of BZK Antiseptic Towelettes (benzalkonium chloride 0.13%) due to manufacturing quality deviations. The towelettes were distributed nationwide under various brand names including Piedmont, Touchpoint, Wellstar Cobb, FSR, and Children's Healthcare of Atlanta labels.

Moderate·FDA·Mar 11, 2026·Acme21 products

Vista Meibo Tears Propylene Glycol 0.6% eye drops were not manufactured under proper safety conditions, raising concerns about sterility. The FDA issued a recall of all lots distributed nationwide. No injuries have been reported.

Moderate·FDA·Mar 4, 2026·Wizcure Pharma7 products

Moisture can get trapped inside these bath foam containers and build up pressure. When opened, pieces may shoot out forcefully and hit someone. The company has received three reports of injuries, including bruises, swelling, and a chipped tooth.

Moderate·CPSC·Feb 26, 2026·Surreal

Medline Industries has recalled multiple sterile surgical kits and procedure trays due to calibration problems in the sterilization equipment used to manufacture them. Although the products went through normal sterilization cycles, the equipment calibration issues may have reduced the sterility assurance level of these kits. No injuries have been reported.

Moderate·FDA·Feb 25, 202642 products

Biomerieux VITEK 2 Gram-negative Susceptibility Cards used to test bacterial resistance to certain antibiotics may produce incorrect results or fail quality control checks. The affected cards test bacteria such as E. coli and Pseudomonas aeruginosa against five antibiotic types. Inaccurate results could lead to inappropriate treatment decisions.

Moderate·FDA·Feb 11, 2026

Cardinal Health is updating instructions for multiple chest drainage unit models to clarify they are intended only for adults 18 years and older. When used on infants, these devices may not show proper bubbling or fluid movement, which can make it hard for clinicians to tell if the device is working correctly. This could delay or prevent needed treatment.

Moderate·FDA·Feb 4, 2026

The buckle on the cargo area bench of these e-bikes can fail to fully latch, which could allow children to fall or shift unsafely during riding. Gazelle USA has received three reports of buckles not latching properly, though no injuries have been reported yet.

Moderate·CPSC·Jan 29, 2026·Gazelle

ICU Medical is recalling three Plum infusion pump models: the Plum Duo Infusion Pump, Plum Duo Precision IV Pump, and Plum Solo Precision IV Pump. In certain cases, the pump's automatic flush feature for piggyback therapy can show a limit violation message that prevents the flush from being programmed. No injuries have been reported.

Moderate·FDA·Jan 28, 20263 products

Gold Star Distribution Inc. distributed multiple food products from a facility where rodents and rodent activity were found. The recall affects snack foods, candy, beverages, baby food, and many other items sold in Indiana, Minnesota, and North Dakota.

Moderate·FDA·Jan 28, 2026

Medline medical procedure convenience kits containing Stryker's Strykeflow 2 Suction Irrigators have a design flaw that allows irrigation solution to leak into the handpiece and battery pack during use. Some devices have leaked fluid or emitted vaporized saline that may resemble smoke during procedures.

Moderate·FDA·Jan 21, 20266 products

Children's Nyquil Cold & Flu (Berry flavor, 8 oz bottles) distributed by Gold Star Distribution has been recalled due to insanitary conditions, including rodent activity, found in their distribution center. All unexpired lots distributed by this company are affected. No injuries have been reported.

Moderate·FDA·Jan 21, 202627 products

ORL Labs is recalling two ORL Kids bubblegum-flavored products: a 16.9 oz mouthwash and a 4 oz natural toothpaste. The products were not made under the required current good manufacturing practices, which are the quality standards for making drugs. The recall covers products distributed only in Arizona, and no injuries have been reported.

Moderate·FDA·Jan 14, 2026·Signature Formulations2 products

A New Life Herbs is recalling its Baby Allergy Herbal Supplement because the product makes drug claims on the label that are not approved by the FDA, and it is missing required Supplement Facts labeling. The product contains echinacea, Oregon grape root, dandelion, burdock root, fenugreek, and ginger root in vegetable glycerin, sold in a 2 oz. glass dropper bottle.

Moderate·FDA·Dec 31, 2025·A New Life Herbs9 products

Myofunctional Research Company USA distributed Myosa for Kids mouthguards in the U.S. without FDA approval. The company mistakenly sold approximately 436 units of these devices, which are designed for children ages 3–15 to help with breathing and myofunctional disorders. No injuries have been reported.

Moderate·FDA·Dec 24, 2025·Myofunctional Research