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Medline convenience kits (models DYNJ48258D and DYNJ48258F) contain Healthmark Instrument Channel Brushes with a potential sharp edge or burr on the brush end. This sharp edge could cause a cut, abrasion, or infection if the brush is handled or used.

Moderate·FDA·Sep 30, 20262 products

SeaSpine Orthopedics is recalling certain Extended Polyaxial Head spinal implants (model MD1-300010-12) because the proximal thread depth does not meet design specifications. This defect could affect the secure attachment of the device during spinal surgery. No injuries have been reported.

Moderate·FDA·Sep 30, 2026

Fresenius Medical Care is issuing a communication regarding its CombiSet hemodialysis blood tubing set (Model 03-2522-1) to ensure healthcare providers and patients review the product's instructions for use. The company is recommending that all treatment preparation and handling steps be performed exactly as instructed to maintain safe operation.

Moderate·FDA·Sep 30, 2026

Maquet PowerLED 300 concealed lighting systems may detach at the connection between the spring arm and suspension arm. This could cause the device to fall and potentially injure someone in an operating room or clinical setting.

Moderate·FDA·Sep 30, 2026

Ventec Life Systems is recalling three HomeFill oxygen cylinder products, 48 units in total. The cylinders do not have the medical gas labeling required by regulators. No injuries have been reported. The recall covers units distributed in Florida, Iowa, Ohio, Nebraska, and Tennessee.

Moderate·FDA·Sep 30, 20263 products

Midmark Corporation's IQvitals Zone vital signs monitor may display inaccurate blood pressure readings when using the Linear Deflation Method. This affects Model 1-200-0320 with Kit 4-000-0622. The device measures blood pressure, pulse, temperature, and oxygen saturation for adult and pediatric patients.

Moderate·FDA·Sep 30, 2026·Midmark4 products

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

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

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

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

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

Whole Foods Market is recalling Fromagerie Coop de Mean Cabricharme and Belgium Cabricharme cheese sold in slices because they contain egg that is not declared on the label. People with egg allergies could have a serious reaction if they eat this cheese.

Serious·FDA·Sep 30, 2026

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·WWF

Kwok Shing American Ginseng products (4 oz and 8 oz packages) may be contaminated with pesticides. The contamination was identified during testing, and 70 boxes have been affected.

Moderate·FDA·Sep 30, 2026·Kwok Shing

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·United Sugar2 products

Evergreen Fresh Sprouts LLC is recalling 4-ounce bags of broccoli sprouts due to potential Salmonella contamination. The affected product was distributed to wholesalers in Washington state in bags with use-by dates between September 7 and September 16, 2026. No illnesses have been reported to date.

Serious·FDA·Sep 30, 2026

Elegant Foods recalled Pecorino Toscano D.O.P. STAGIONATO cheese wheels (approximately 3–4 lbs each) produced in Italy due to potential Listeria contamination. The contamination may have occurred from dripping condensation in the storage cooler. The recall affects Lot 093DPD distributed in Wisconsin.

Moderate·FDA·Sep 30, 2026

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

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

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

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

MENOW Sunscreen Pressed Powder SPF35 PA+++ was manufactured in ways that do not meet U.S. cosmetic manufacturing standards (cGMP deviations). The affected product was distributed in California only. No injuries have been reported.

Moderate·FDA·Sep 30, 2026·Shantou Qiwei

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

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·Unilever

The high-voltage battery in certain 2023–2026 Volkswagen ID.4 vehicles may fail, creating a risk of vehicle fire and injury. Volkswagen is developing a repair and has advised owners to charge only to 80% capacity until the fix is available.

Serious·NHTSA·Sep 30, 2026

Certain Greenpower EV Star and EV Star Mobility Plus buses made between 2018 and 2024 have a software error that may allow the bus to move while a wheelchair lift is deployed. This creates a risk of injury to passengers using the lift.

Moderate·NHTSA·Sep 30, 2026·Greenpower Motor Company Inc.

Certain 2026–2027 Grech Motors Strada, Terreno, and Turismo motorhomes have MaxxAir N-Series rooftop ventilation fans with a printed circuit board that may overheat and fail. An overheated circuit board creates a fire risk.

Moderate·NHTSA·Sep 30, 2026·Grech Motors Inc.

The fresh water tank on certain 2022–2024 Range Lite Air travel trailers may detach due to fastener failure. A loose tank can fall onto the road and become a hazard to other vehicles.

Moderate·NHTSA·Sep 30, 2026·Highland Ridge RV

Fasteners on certain 2022–2024 Starcraft Super Lite Maxx travel trailers may fail, causing the fresh water tank to detach. A loose tank can fall onto the road and create a hazard for other vehicles.

Moderate·NHTSA·Sep 30, 2026·Starcraft RV

Certain 2027 Rivian R2 vehicles have a high voltage battery fastener that may not have been tightened properly during manufacturing. This can cause a sudden loss of drive power while driving, which increases the risk of a crash.

Serious·NHTSA·Sep 29, 2026·Rivian Automotive, LLC