Minnesota recalls

Sold nationwide. Some Olympus EZDilate Endoscopic Balloon Dilator devices (Model BD-420X-1355) have an incorrect label on the shaft. The inflation chart label may show balloon sizes of 18, 19, or 20 mm when the actual device is 11, 12, or 13 mm. This mislabeling could lead to confusion during use.

Moderate·FDA·Sep 30, 2026·Olympus

Sold nationwide. The wheels on Heidelberg Engineering's SPECTRALIS imaging device may come loose when the module is pushed or pulled during movement or transportation. If wheels loosen, the stand can become unstable and tip over, potentially causing impact or crushing injuries to nearby people.

Moderate·FDA·Sep 30, 2026·Heidelberg Engineering

Sold nationwide. The tip of certain Boston Scientific Imager II Angiographic Catheters may fracture or detach during use. Fragments could remain in the patient's body or travel through blood vessels, potentially causing a prolonged procedure or life-threatening blood clot.

Serious·FDA·Sep 30, 2026·Boston Scientific

Sold nationwide. CooperSurgical is recalling two INCA infant nasal CPAP product lines, 2,792 boxes (13,960 units) in total, because the flexible tubing may loosen from the nasal cannula during assembly or use. A loose connection can cause a loss of CPAP pressure, which may reduce treatment effectiveness and lower oxygen levels until the connection is restored. No injuries have been reported.

Serious·FDA·Sep 30, 2026·CooperSurgical2 products

Sold nationwide. bettergoods Lemon Alfredo Fettuccine pasta distributed by Walmart may be contaminated with Listeria monocytogenes, a harmful bacteria. The affected product was made in Italy and sold nationwide at Walmart locations. No illnesses have been reported so far.

Serious·FDA·Sep 30, 2026·bettergoods

Sold nationwide. So Delicious Dairy Free Salted Caramel Cluster Cashewmilk (16 oz tubs) may contain small stones or other hard objects. The product was distributed nationwide. No injuries have been reported.

Moderate·FDA·Sep 30, 2026·So Delicious Dairy Free

United Sugar Producers & Refiners is recalling two 50-pound sugar products because they may contain wheat kernels. The products are light brown sugar (item 810051) and United 6X powdered sugar (item 810087), sold under the United name and at least one other brand. The products were distributed in IA, IL, IN, KS, MN, OH, PA, and TX. No injuries have been reported.

Moderate·FDA·Sep 30, 2026·Good & Gather2 products

Sold nationwide. Prestige Consumer Healthcare is recalling 2 products, both Clear Eyes Redness Relief lubricant and redness reliever eye drops in 0.5 fl oz (15 mL) bottles, one sold with a hang tag. The company cannot assure the drops are sterile. No injuries have been reported, and about 2.4 million bottles were affected.

Moderate·FDA·Sep 30, 2026·Prestige Consumer Healthcare2 products

Sold nationwide. Some prefilled pens of Amneal Exenatide Injection may contain no medication due to a defective delivery system. This affects lot AP250095A (expiration 2/28/2027). Patients relying on these pens may not receive their intended dose.

Moderate·FDA·Sep 30, 2026·Amneal Pharmaceuticals

Sold nationwide. Macleods Pharmaceuticals has recalled Olanzapine Tablets USP 5 mg (lot BOB22321A, expiring 07-31-2027) because testing found organic impurities above acceptable limits. The affected bottles were distributed nationwide. No injuries have been reported.

Moderate·FDA·Sep 30, 2026·MacLeods Pharma

Sold nationwide. The FDA has announced a nationwide recall of 9 lubricant eye drops and one eye ointment sold under the Walgreens, AvKare, Reliable-1 Laboratories, TRP Gentle Eyes, Major LubriFresh P.M. and Cameron Pharmaceuticals names. The manufacturer could not confirm that the products are sterile, which is required for eye products. No injuries have been reported.

Moderate·FDA·Sep 30, 2026·Sterling Pharmaceutical Services9 products

Sold nationwide. ICU Medical's 0.9% Sodium Chloride Injection (100 mL) may be mislabeled. Some bags marked as sodium chloride may actually contain potassium chloride instead. This mix-up affects lot 1042188, expiring 10/31/2027, distributed nationwide.

Serious·FDA·Sep 30, 2026·ICU Medical

Unilever's Almond Joy Ice Cream Bars (2.0 fl. oz.) have inaccurate Nutrition Facts information printed on the packaging. The affected products are 6-bar cartons distributed across the United States. No injuries have been reported.

FDA·Sep 30, 2026·Almond Joy

Sold nationwide. A specific lot of Mezzetta Golden Greek Peperoncini Medium Heat (32 oz.) may contain a pest contaminant in the jar. The company identified the issue after a consumer video circulated on social media and immediately launched a voluntary recall of the affected lot. No illnesses or injuries have been reported.

Moderate·FDA·Sep 26, 2026·Mezzetta

Sold nationwide. ABC Trading's light-up toys (ties, headbands, and glasses) contain button cell batteries in compartments that children can easily open. Swallowing these batteries can cause serious internal injuries, chemical burns, and death.

Serious·CPSC·Sep 24, 2026·ABC Trading

Sold nationwide. Love To Dream portable sleep machines contain a lithium-ion battery that can overheat if an incompatible charger is used. This overheating poses a risk of fire or burns.

Moderate·CPSC·Sep 24, 2026·Love To Dream

Sold nationwide. The left temple of INMO Air3 Smart Glasses can overheat during extended use, causing burns to the face and ear. The company has received 10 reports of overheating, including burning sensations. The affected glasses were sold online between December 2025 and August 2026.

Serious·CPSC·Sep 24, 2026·INMO

Sold nationwide. Style Homeware Emerspring mattresses sold on Amazon do not meet federal flammability standards for mattresses. This poses a risk of serious injury or death if a fire occurs near the mattress.

Serious·CPSC·Sep 24, 2026·Style Homeware

Sold nationwide. These wooden dressers can tip over if not anchored to the wall, creating a serious injury or death risk for children. The dressers don't meet federal safety standards for furniture stability.

Serious·CPSC·Sep 24, 2026·Keben

Sold nationwide. Xinan Home WinxMatrs twin-size mattresses do not meet federal flammability standards and pose a risk of serious injury or death from fire. The black, 10-inch-thick mattresses were sold compressed in boxes on Amazon from August through November 2025.

Serious·CPSC·Sep 24, 2026·Xinan Home

Sold nationwide. NEWDERY power banks with model number ZHX-PB22 (black with yellow cables) can have lithium-ion batteries that unexpectedly explode or catch fire. The company has received nine reports of fires, including one that caused $2 million in property damage and one burn injury.

Serious·CPSC·Sep 24, 2026·NEWDERY

Sold nationwide. The lithium-ion battery packs in Blue Cactus Company Reclining Chair model RWX-RBP02 can overheat and catch fire or cause burns. About 51,000 units were sold on Amazon between May 2023 and July 2026. The company has received four reports of batteries overheating, smoking, or igniting.

Serious·CPSC·Sep 24, 2026·The Blue Cactus

Sold nationwide. 5Color size-small bicycle helmets in children's helmet and pads sets do not meet mandatory federal safety standards. The helmets may fail to protect a child's head in a crash, creating a serious risk of injury.

Serious·CPSC·Sep 24, 2026·5Color

Sold nationwide. Kesyup-branded mattresses sold on Amazon do not meet mandatory U.S. flammability standards for mattresses. The mattresses are 12 inches thick, available in twin, full, queen, and king sizes, and have a white top with blue sides and trim. They were sold in compressed boxes from December 2024 through April 2026.

Serious·CPSC·Sep 24, 2026·ZCK01

Sold nationwide. Pi-Cardia Inc. identified a weld issue in the ShortCut transfemoral catheter that may cause the positioning arm to detach during use. The defect affects 46 units in specific serial number lots distributed across eight U.S. states. No injuries have been reported to date.

Moderate·FDA·Sep 23, 2026·PI Cardia

Sold nationwide. ICU Medical's CADD Yellow Medication Cassette Reservoirs may leak medication at the connection point between the luer connector and tubing. This leakage could delay or stop medication delivery, reduce the amount of medication received, expose patients to contamination, or allow air to enter the bloodstream.

Serious·FDA·Sep 23, 2026·ICU Medical

Sold nationwide. Reign Medical's Clench Staple System (Compression) was distributed without adequate performance testing and requires additional FDA clearance. The device is used in bone fixation procedures. About 600 units were distributed nationwide.

Moderate·FDA·Sep 23, 2026·Foundation Medicine

Sold nationwide. Medline is recalling four convenience kit products because some kits may have open seals in their sterile pouch packaging. An open seal may compromise sterility, which could lead to contamination of a sterile field or patient infection if the kit is used. The recall covers 1,196 affected units distributed nationwide, with distribution listed in Arkansas, Florida, North Carolina, Maryland, and Texas.

Moderate·FDA·Sep 23, 2026·Medline4 products

Sold nationwide. Howmedica Osteonics is recalling 12 orthopaedic implant components made from polyethylene material that was aged more than five years before use. The aged material may oxidize, which can increase wear and lead to wear debris, fractured or dislodged parts, and may require revision surgery. No injuries have been reported.

Moderate·FDA·Sep 23, 2026·Howmedica Osteonics12 products

Sold nationwide. The tension bolt in certain Mirion Captus 4000e thyroid imaging systems can fail, allowing the spring arm to unexpectedly drop to its lowest position, about 25 inches from the ground. This affects specific models shipped between April 2019 and February 2024 that have not yet received the redesigned arm. No injuries have been reported.

Moderate·FDA·Sep 23, 2026·Mirion Technologies