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Wonton Specialist Inc. wonton skins (16 oz packages) contain FD&C Red No. 40, a food dye that was not declared on the label. This poses a risk to people with allergies or sensitivities to this dye. About 480 bags were distributed in New York, New Jersey, and Pennsylvania.

Moderate·FDA·Sep 9, 20266 products

Weis Markets' Fresh From the Orchard Pasteurized Apple Cider contains unsafe levels of patulin, a naturally occurring toxin found in apples. The recalled product was distributed in Pennsylvania in pints, half-gallons, and gallon jugs with expiration dates between July 17 and September 30, 2026.

Moderate·FDA·Sep 9, 2026

Prince Bakery is recalling four bread products because sesame is named in the product name but not listed in the ingredient statement. The products are Prince Italian Bread (8 oz and 12 oz), Prince Sesame French Bread (10 oz), and Prince Pan de Manteca Spanish Style (8 oz). The recall covers products distributed in New York. No illnesses or injuries have been reported.

Moderate·FDA·Sep 9, 20264 products

American Health Packaging distributed buprenorphine sublingual tablets with incorrect labeling. The affected medication is a prescription opioid used to treat pain and opioid use disorder. A label mix-up could result in dosing errors if patients or healthcare providers rely on incorrect information.

Moderate·FDA·Sep 9, 2026·American Health Packaging

Mylan Pharmaceuticals is recalling Prasugrel 10mg tablets (Lot #3225272, expiring September 30, 2026) because they failed dissolution testing during 18-month stability studies. This means the tablets may not break down and release the medication as intended in the body. No injuries have been reported.

Moderate·FDA·Sep 9, 2026

Chiesi USA, Inc. is recalling Revcovi (elapegademase-lvlr) Injection due to out-of-specification stability results in the protein concentration profile. The affected lot was distributed to Missouri and Tennessee. No injuries have been reported.

Moderate·FDA·Sep 9, 2026

Sage Products is recalling specific lots of 2% Chlorhexidine Gluconate non-sterile cloths due to potential cross-contamination with other products during manufacturing. The affected cloths may not meet safety and quality standards. No injuries have been reported.

Moderate·FDA·Sep 9, 2026·Sage Products

Teva Pharmaceuticals discovered that some bottles of trazodone 50 mg tablets contain foreign tablets or capsules mixed in with the correct medication. The issue affects one lot (1394026) with an expiration date of February 2028. No injuries have been reported.

Moderate·FDA·Sep 9, 2026

Supernus Pharmaceuticals is recalling one lot of Trokendi XR (topiramate) 50 mg extended-release capsules because the medication did not dissolve as designed. When a medication fails to dissolve properly, the body may not absorb the full dose, potentially reducing its effectiveness.

Moderate·FDA·Sep 9, 2026·Supernus

Mylan Pharmaceuticals is recalling specific lots of Mycophenolate Mofetil for injection (500 mg/vial) because the medication failed to meet dissolution specifications—meaning the drug may not dissolve properly in the body. This could affect how well the medicine works. The recall affects two lots distributed nationwide.

Moderate·FDA·Sep 9, 2026

The FDA recall covers two Broadway Joe's pain creams containing CBD and hempseed oil, sold in 2 oz and 4 oz jars. The recall was made because of possible contamination of a raw material, found through manufacturing quality issues. The products were distributed in Colorado, and no injuries have been reported.

Moderate·FDA·Sep 9, 2026·Lexia2 products

Allies is recalling four sizes of THE ONE SPF 50 Invisible Sunscreen Gel, sold as 3 mL sachets, 20 mL, 50 mL and 90 mL tubes. Testing found the product may not reliably provide the SPF 50 protection stated on the label. No injuries have been reported.

Moderate·FDA·Sep 9, 2026·Allies4 products

Bionpharma Inc. is recalling Doxylamine Succinate and Pyridoxine HCl Delayed-Release tablets (10 mg/10 mg, 100-count bottles) because some bottles contain unidentified foreign tablets or capsules mixed in with the correct medication. The affected lot is DMA25006 with an expiration date of 11/30/2028. This issue was discovered during quality control.

Moderate·FDA·Sep 9, 2026·Bionpharma

Baxter is recalling 17 intravenous (IV) drug products for manufacturing quality problems, called CGMP deviations, which are lapses in the required production standards. The products include vancomycin, daptomycin, clindamycin, famotidine, dexmedetomidine, vasopressin, pantoprazole, insulin, nicardipine, and amiodarone, plus the brand names Myxredlin, CARDENE IV, and Nexterone. They were distributed nationwide, in Puerto Rico, and in Chile, and no injuries have been reported.

Moderate·FDA·Sep 9, 202617 products

Golden State Medical Supply Inc. is recalling Prasugrel HCI 10mg tablets (lot GS062298, expiration 09/30/2026) because they failed to meet dissolution specifications during quality testing. Dissolution is how quickly a tablet breaks down in the body to release its active ingredient. Tablets that dissolve too slowly or incompletely may not work as intended.

Moderate·FDA·Sep 9, 20262 products

Certain 2026 Ford Explorer vehicles have a passenger-side air bag vent that may not open as intended, which could prevent the air bag from deploying during a crash. This increases the risk of injury to passengers in a collision.

Moderate·NHTSA·Sep 9, 2026

Certain 2026 Ford Broncos have a mounting bracket on the right-hand side curtain air bag with a metal burr that can tear the air bag during deployment. A torn air bag may not properly restrain an occupant in a crash, increasing injury risk.

Moderate·NHTSA·Sep 9, 2026

The wireless seat belt reminder system in the rear seat belt buckles of certain 2026-2027 Ford Transit vehicles may malfunction and fail to alert occupants when a seat belt is unfastened. This increases the risk of injury in a crash.

Moderate·NHTSA·Sep 9, 2026

Certain 2026 Ford F-150 vehicles have stabilizer rod fasteners that may not have been properly tightened during manufacturing. This can allow the rod to shift out of position, reducing vehicle handling and control and increasing crash risk.

Moderate·NHTSA·Sep 9, 2026

Certain 2026 Ford F-150 vehicles were built with an incorrect rear axle tail bearing. This defect can cause the rear wheels to lock up, making the vehicle hard to control, or cause the driveshaft to separate, resulting in loss of power or the vehicle rolling away if parked without the parking brake.

Moderate·NHTSA·Sep 9, 2026

The touchscreen instrument cluster in certain 2024–2027 Can-Am motorcycles may reset, freeze, or go blank, leaving the display unable to show vehicle speed and warning lights. This increases the risk of a crash.

Moderate·NHTSA·Sep 7, 2026·Bombardier Recreational Products, Inc.

Certain 2026–2027 Kibbi recreational vehicles equipped with MaxxAir rooftop ventilation fans may have a printed circuit board that can fail and overheat during normal operation. An overheated circuit board creates a fire risk.

Moderate·NHTSA·Sep 5, 2026·Kibbi, LLC

A coolant sensor in certain 2023–2024 Nova Bus LFS Artic and 2022–2024 LFS buses can send a false signal, causing the engine to shut down without warning. An unexpected shutdown increases crash risk and can create unsafe conditions when passengers need to be transferred from a disabled bus.

Moderate·NHTSA·Sep 3, 2026

Clorox Puerto Rico is recalling about 6.3 million bottles of scented Mistolin and Lestoil cleaners sold in Puerto Rico and the U.S. Virgin Islands. The products may contain Pseudomonas aeruginosa bacteria, which can cause serious infections in people with weakened immune systems or external medical devices if the bacteria is inhaled, touches the eyes, or enters through a break in the skin. People with healthy immune systems are typically unaffected.

Moderate·CPSC·Sep 3, 2026·Clorox

The backrests on certain Branch height-adjustable ergonomic chairs can detach due to incorrectly installed anchors at the factory. This poses a fall hazard. The chairs were made between September 10, 2025 and April 22, 2026. Branch has received 11 reports of backrest detachment but no injuries so far.

Moderate·CPSC·Sep 3, 2026

A software update to GE's Portrait Compute and Core Services system may cause patient monitoring to stop working at the Hub and Central Viewer. The update can also reset all alarm settings back to factory defaults, overriding the alarm configurations that were previously set up for individual patients or care areas.

Moderate·FDA·Sep 2, 20264 products

Olympus Corporation of the Americas is recalling POWERSEAL 5mm curved jaw sealer and divider devices due to incorrect labeling on the outer box. Some units labeled as 37 cm devices actually contain 23 cm devices, which could lead to confusion during surgical use. The issue affects 335 units distributed in the US, Australia, the European Union, and Japan.

Moderate·FDA·Sep 2, 2026

Healthmark Industries is recalling two ProChek protein test products, 5,143 units in total. The tests were made with an expired ingredient, so they may give false negative or false positive results. No injuries have been reported.

Moderate·FDA·Sep 2, 2026·Healthmark Industries2 products

FUJIFILM Synapse PACS software version 7.4.310, used in radiological imaging systems, has a software issue that can cause the ruler measurement tool to display inaccurate values. This affects 6 units distributed across select US states and Australia. No injuries have been reported.

Moderate·FDA·Sep 2, 2026·Fujifilm

Medline is recalling 11 groups of surgical convenience kits. The kits contain a component that the manufacturer recalled because it may be contaminated. No injuries have been reported, and the kits were distributed in 18 states.

Moderate·FDA·Sep 2, 202611 products