Hawaii recalls

Sold nationwide. Pearl Milling Company Original Pancake & Waffle Mix Complete is being recalled because it contains undeclared milk and soy, which are not listed on the label. The product was distributed only in Puerto Rico. No injuries have been reported.

Serious·FDA·Jul 1, 2026·Pearl Milling Company

Sold nationwide. Spring & Mulberry is recalling 11 flavors of its 2.1 oz date-sweetened chocolate bars, including Mint Leaf, Mixed Berry, Earl Grey, Pure Dark, Pecan Date, and Blood Orange, because they may be contaminated with Salmonella. The bars were sold nationwide, and no illnesses have been reported.

Serious·FDA·Jul 1, 2026·Spring & Mulberry11 products

Sold nationwide. Motor City Pizza Co. 5 Cheese Bread products may contain Salmonella, a bacteria that can cause serious illness. The affected products were distributed nationwide to major retailers including Costco, Walmart, Target, and Kroger.

Moderate·FDA·Jul 1, 2026·Motor City Pizza Co

Prime Food Processing dried herring fish (7 oz.) was not properly cleaned before drying, which can allow Clostridium botulinum bacteria to grow. This bacterium produces a toxin that causes botulism, a serious foodborne illness. The affected product has lot code 26020 with expiration date 06.12.28.

Serious·FDA·Jul 1, 2026·Prime Food Processing

Sold nationwide. Sun Pharmaceutical discovered that some bottles labeled as containing 6mg Perampanel tablets actually contained 10mg tablets instead. This mix-up affects one lot (AE01763) distributed nationwide. Patients taking the wrong strength could receive an incorrect dose of this seizure medication.

Moderate·FDA·Jul 1, 2026·Sun Pharmaceutical

Sold nationwide. Elevate Oral Care's Povi-One 10% Povidone-Iodine Oral Antiseptic does not contain the full strength stated on the label. Five specific production lots distributed nationwide do not meet the required potency standard, which means the product may not work as intended for oral antiseptic purposes.

Moderate·FDA·Jul 1, 2026·Elevate Oral Care

Sold nationwide. Some bottles of Lacosamide 100mg tablets may contain Selexipag 1000 mcg tablets instead. This mix-up happened during manufacturing and could cause patients to take the wrong medication. The recall affects specific lots distributed nationwide.

Moderate·FDA·Jul 1, 2026·Annora Pharma

Sold nationwide. CareFusion is recalling four sizes of BD ChloraPrep Clear and BD ChloraPrep FREPP Clear skin antiseptic applicators because wrinkles in the paper lid may break the seal, so the products may not stay sterile. No injuries have been reported. The products were distributed nationwide in the U.S. and to other countries.

Moderate·FDA·Jul 1, 2026·CareFusion4 products

Sold nationwide. ANI Pharmaceuticals is recalling hydroxyzine hydrochloride oral solution (10 mg/5 mL, 473 mL bottles) due to the presence of a foreign substance in one lot. The affected product was distributed nationwide. No injuries have been reported.

Moderate·FDA·Jul 1, 2026·ANI Pharmaceuticals

Sold nationwide. Direct Rx's packaged Duloxetine D/R 30 mg capsules contain levels of N-nitroso-duloxetine, a potentially harmful impurity, above FDA's recommended limit. This is a manufacturing quality issue affecting specific lots distributed nationwide.

Moderate·FDA·Jul 1, 2026·Direct Rx

Sold nationwide. Amgen is recalling five bottle sizes of two prescription heart and thyroid-related drugs, Corlanor (ivabradine) and Sensipar (cinacalcet), because the tablets may contain a foreign substance. The products were distributed nationwide, and no injuries have been reported.

Moderate·FDA·Jul 1, 2026·Amgen5 products

Sold nationwide. Ajanta Pharma USA Inc. is recalling one lot of fenofibrate 200 mg capsules due to manufacturing quality deviations discovered during inspection. The affected lot (PA02216, expiring 12/2029) was distributed nationwide.

Moderate·FDA·Jul 1, 2026·Ajanta Pharma

Sold nationwide. MAJOR Pharmaceuticals is recalling Methylergonovine Maleate Tablets, USP, 0.2 mg due to subpotency — meaning the tablets contain less active ingredient than labeled. The affected lots were distributed nationwide. This is a prescription medication used to control bleeding after childbirth.

Moderate·FDA·Jul 1, 2026·The Harvard Drug

Sold nationwide. Revival Animal Health is recalling several canine and goat milk replacer products because they contain inconsistent levels of vitamin D—some too low, some too high. Dogs fed these products may develop serious health problems ranging from vomiting and weakness to bone deformities (rickets in puppies) or kidney damage (from excess vitamin D). Two cases of rickets have been reported so far.

Serious·FDA·Jun 25, 2026·Revival Animal Health

Sold nationwide. Treatlife smoke and carbon monoxide detectors can fail to sound an alarm when smoke or fire is detected. These white, circular detectors are powered by AA batteries and were sold on Amazon. The failure to alert poses a risk of serious injury or death from smoke inhalation or burns.

Serious·CPSC·Jun 25, 2026·Treatlife

Sold nationwide. Certain Amana brand window and through-the-wall air conditioners and heat pumps can experience a ground fault that leaves the heating element energized even after the unit is turned off. This poses a risk of fire or burn injury. One report of plastic melting on a unit has been received, though no injuries have occurred so far.

Serious·CPSC·Jun 25, 2026·Daikin

Sold nationwide. Honlyne LED party favors sold on Amazon contain button cell batteries in compartments that children can easily access and swallow. Swallowing these batteries can cause serious internal injuries, chemical burns, and death.

Serious·CPSC·Jun 25, 2026·ABGA Advanced Trading

Sold nationwide. Small Fish Montessori Busy Board toys (model 2512JX02) contain 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 injury or death from intestinal perforation, blockage, or infection.

Serious·CPSC·Jun 25, 2026·Small Fish

Sold nationwide. These light-up sneakers contain coin batteries that children can easily access and swallow. Ingesting these batteries can cause serious internal burns and other life-threatening injuries. The sneakers lack required safety warnings and do not meet federal battery safety standards.

Serious·CPSC·Jun 25, 2026·Carina

Sold nationwide. MedPride Baby Oil bottles do not have child-resistant caps as required by law. Young children can open the bottle and swallow the oil, which contains petroleum distillates that can cause serious poisoning, chemical pneumonia, and potentially fatal lung damage.

Serious·CPSC·Jun 25, 2026·Shield Line

Sold nationwide. The Lomi Roll-On Waxing Kit (models LOMB2003PK and LOMB2004PK) does not meet safety standards for flammability and presents a risk of burns or fire. These handheld wax warmers were sold online through Amazon from October 2020 through January 2026. About 14,700 units are affected.

Serious·CPSC·Jun 25, 2026·Veseacky

Sold nationwide. The lithium-ion battery in the Super Off-Road 12,000 mAh Solar Wireless Power Bank can swell and overheat, creating a burn hazard. The company has received two reports of battery swelling. About 7,400 units were distributed as promotional items between January 2019 and December 2023.

Moderate·CPSC·Jun 25, 2026·Spector

Sold nationwide. Yamazuki's Sunderwell brand youth ATVs (model XW-A17) sold online lack brake lights, making them harder for other vehicles to see. This visibility gap increases the risk of crashes and serious injury. About 200 units were sold between October and December 2025.

Serious·CPSC·Jun 25, 2026·Yongkang Ruihe

Sold nationwide. Kith Retail recalled children's loungewear sets in black and red plaid print because they don't meet federal flammability standards for children's sleepwear. The pajamas pose a risk of serious burn injuries. The sets were sold at Kith stores and online from December 2025 through January 2026.

Serious·CPSC·Jun 25, 2026·Kith

Sold nationwide. Thoratec is recalling three HeartMate products: HeartMate 3 Left Ventricular System kits, System Controllers, and HM 11V Li-ion Backup Batteries. The 11-volt backup batteries can fail. No injuries have been reported.

Serious·FDA·Jun 24, 2026·Thoratec3 products

Sold nationwide. Merit Medical Systems' Splashwire Hydrophilic Guide Wire — used by doctors in vascular procedures — has been recalled because some product pouches were not sealed properly. Unsealed pouches can allow contamination or damage to the sterile device before use.

Moderate·FDA·Jun 24, 2026·Merit Medical

Sold nationwide. Inspire Medical Systems is recalling two implant lead products, the Respiratory Sensing Lead and the Stimulation Lead, because they carry a Use By Date that goes beyond their validated three-year shelf life. The agency says material can degrade past the labeled date, which may lead to unplanned or premature revision surgery. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·Inspire2 products

Sold nationwide. A firmware bug in the iLet Bionic Pancreas can cause the lock screen to fail to unlock when users slide the unlock slider. When this happens, users become stuck on the lock screen and cannot change insulin cartridges or enter meal information. The pump will continue delivering insulin until the cartridge empties and the battery drains, which may lead to high blood sugar.

Moderate·FDA·Jun 24, 2026·Beta Bionics

Sold nationwide. Staar Surgical's ICL Calculation Software Version 8.00 contains a coding error that can produce incorrect implantation orientation diagrams for toric intraocular lenses. The error occurs when multiple toric lens calculations are generated for the same eye between April 13–16, 2026. An incorrect diagram could lead to improper lens alignment during surgery.

Moderate·FDA·Jun 24, 2026·Staar Surgical

Sold nationwide. Medline recalled 30 products, including urethral catheters, catheterization trays, intermittent latex catheters, and medical procedure kits. During an internal review, the company found that some samples did not meet performance specifications, including surface irregularities, connectors that detached early from the catheter funnel, and some catheters with outer diameters outside specification. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·Medline30 products