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Olympus is recalling four BiCOAG Hemostasis Probe models because they may have been made without the full amount of adhesive, so the ceramic tip could detach. The recall covers 3,467 units sold in the US and several other countries. No injuries have been reported.

Moderate·FDA·Sep 30, 20264 products

Philips is recalling 12 groups of MRI systems and related upgrade products because of a software issue. If scan settings are manually adjusted so the image processing needs more memory than the system has, the examination can end partway through. No injuries have been reported.

Moderate·FDA·Sep 30, 202612 products

Some units of the Biomerieux VITEK 2 AST-N461 test kit used to determine antibiotic susceptibility in gram-negative bacteria have damaged card pouches. This damage can cause the test to report false resistant results, which may lead to use of less effective antibiotics or unnecessary antibiotic combinations.

Moderate·FDA·Sep 30, 2026

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

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

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·Good & Gather2 products

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

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 2022–2023 Nova Bus LFS transit buses have mounting screws that may be too short, causing the bike rack to strip and detach. A loose bike rack can fall onto the road and create a hazard for other vehicles.

Moderate·NHTSA·Sep 29, 2026

Certain 2026 Ram 1500 vehicles have tire pressure sensors that may fail to detect low tire pressure or illuminate the warning light. This prevents drivers from being alerted to dangerous tire conditions, increasing crash risk.

Moderate·NHTSA·Sep 29, 2026

Water can enter the electric power steering wiring harness in certain Chrysler MOPAR body and jumper wiring harnesses, disabling power steering assist. Loss of power steering makes the vehicle harder to steer and increases crash risk.

Moderate·NHTSA·Sep 29, 2026

Certain 2026–2027 Mack Anthem and Pioneer trucks with tanker packages have a software error that miscalculates axle load. This can reduce braking performance, especially when towing smoothbore tanker trailers, making the truck require a longer distance to stop.

Moderate·NHTSA·Sep 28, 2026

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

Certain 2021–2026 Altec Digger Derrick and 2023–2025 Altec TA Series vehicles have improper wiring in the power distribution module. This wiring defect can prevent the boom stow auto-neutral system from working, which means the truck may be driven with the boom still raised and unsecured.

Moderate·NHTSA·Sep 24, 2026