Recall archive
Recalls, week of Jul 6, 2026
38 recalls from July 6, 2026 to July 12, 2026. Urgent ones come first.
FDA Class IFDA·Medical devices A part of the pod that delivers insulin was damaged during manufacturing, so insulin can leak around the pod instead of reaching the user, which can cause high blood sugar, DKA, HHS or even death.
Insulet Corporation · 7,015,886 units

The powdered infant formula may be contaminated with Clostridium botulinum, a bacterium, and the notice covers 377,610 cans sold nationwide in 24.7 oz and 14.1 oz sizes.
Nara Organics INC · 377,610 cans
The company stopped the required stability testing on these products, which are still within their expiry dates, so it cannot show they stay safe and effective until they expire.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Blaine Labs Inc · 63,308 units
FDA Class IFDA·Supplements The notice says the MOGO Pure Moringa Oleifera capsules, 180 quick release veggie capsules, may be contaminated with Salmonella Typhimurium, and 23,186 bottles were sold nationwide online.
MOGO Moringa LLC · 23,186 bottles
The tempered glass window in the grill's pizza oven can shatter during use, which could cause serious cuts, and the company has received 37 reports of shattered glass but no injuries.
Conair LLC, of Stamford, Connecticut, dba Cuisinart · About 12,660 units



The lithium-ion battery in these power banks can overheat and catch fire, which could cause serious injury or death, and the company has received five reports of overheating and fires, including two burns.
iDecoz Inc. dba Flaunt, of Brooklyn, New York · About 1,400 units



The 9 oz bags of FIRST STREET Dark Chocolate Raisins may contain peanuts that are not listed on the label, which matters for anyone with a peanut allergy.
Western Mixers Produce & Nuts, Inc. · 29 cases
The notice says the prednisoLONE Acetate Ophthalmic Suspension, USP, 1% in 5 mL, 10 mL and 15 mL bottles may contain a foreign substance, and 2,530,182 bottles were sold across the U.S.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Lupin Pharmaceuticals Inc. · 2,530,182 bottles
These Subaru vehicles were built with the wrong maximum axle weight rating on their certification label, which could lead owners to overload them and raise the risk of a crash.
Subaru of America, Inc. · 541,237 vehicles
The labels carry a symbol saying the plug contains no DEHP, a plastic-softening chemical, but the plug actually contains 30 to 35% DEHP.
Covidien LLC · 293,659 devices
Some of these feeding tube extension sets may have the wrong connectors, so they will not attach to ENFit connections, which could slightly delay delivery of liquid nutrition or oral medication.
Medela Inc · 82900 units
During 12-month long term stability testing, the kit's diluent syringe gave an out-of-specification result on the Gliding Force functionality test, which the notice calls a CGMP deviation.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Lupin Pharmaceuticals Inc. · 64,894 units
The vegan nuggets and sausage patties may be contaminated with plastic material, which could be a risk if someone eats a piece of it.
Mars Snacking · 38,332 units
The tablets contain N-nitroso-cinacalcet, an impurity, at a level above the acceptable daily intake, and the notice lists manufacturing practice deviations as the reason.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Cipla USA, Inc. · 31,824 units
The tablets failed impurity and degradation specifications, meaning they did not meet required standards for what the medicine should contain as it ages.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Sun Pharmaceutical Industries INC · 9,048 bottles
The Vista MAX dietary supplement contains Yellow #5 that is not listed on the label, which matters for anyone who needs to avoid that dye.
Provision Health Corp. dba PH Labs · 6,967 units across all lots
The recalled levothyroxine tablets are subpotent, meaning they contain less medicine than the label says, so they may not work as well as intended.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Accord Healthcare, INC. · 6432 bottles
The rear brake caliper can crack when the motorcycle rolls backwards and may break while riding, which can reduce braking ability and raise the risk of a crash.
KTM North America, Inc. · 6,257 vehicles
The rear axle carriers may have been made with insufficient material strength and could break, which can cause a sudden loss of vehicle stability and control and raise the risk of a crash.
Toyota Motor Corporation · 5,408 vehicles
The lights may not illuminate properly, which can make a trailer harder for other drivers to see and raise the risk of a crash.
Harbor Freight Tools · 3,832 pieces of equipment
The capsules are labeled as extended-release (ER) but contain only immediate-release (IR) pellets, so the label does not match what is inside.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Lannett Company Inc. · 1392 bottles
The pepperoni rolls contain milk that is not listed on the label, which could cause a serious reaction in people allergic to milk, and they were not kept refrigerated as required.
Fry Pie Factory LLC · 850 individual units
The wrong detergent was used and required swab testing was skipped when cleaning a production hopper that had earlier held a different product, so the tablets may not meet manufacturing standards.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Boehringer Ingelheim Pharmaceuticals, Inc. · 560 bottles
The circuit board in certain MaxxAir N-Series Maxxfan rooftop ventilation fans can fail during certain operations and overheat, which raises the risk of a fire.
Grand Design RV, LLC · 448 vehicles
The notice says there is a lack of assurance of sterility for 326 single dose vials of IMULDOSA (ustekinumab-srlf) Injection, 130 mg/26 mL (5mg/mL), sold across the US.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Accord Biopharma INC · 326 vials
The recalled 1-gallon plastic pails of Blue Ribbon Classics French Vanilla, with a blue label, were found to have elevated coliforms, and 195 cases went to one customer in Kenosha, WI.
Wells Enterprises, Inc. · 195 cases
The software may not detect heavy smoke and could let the vehicle drive into low-visibility areas such as active emergency scenes, which can raise the risk of a crash or get in the way of first responders.
Zoox, Inc. · 105 pieces of equipment
The federal placard on these travel trailers may list the wrong maximum weight rating, which could lead owners to overload the trailer and raise the risk of a crash.
Forest River, Inc. · 18 vehicles
These 15 cars were built for a foreign market, so they lack knee air bags and may lack other interior safety features, which could raise the risk of injury in a crash.
Tesla, Inc. · 15 vehicles
The Q'Straint Max wheelchair retractors in certain vans may not lock, so a wheelchair may not be properly secured and could move during a trip, raising the risk of injury.
American Seating Company · 12 pieces of equipment
The fuel fill line on these vehicles may be missing a braze connection, which could let fuel leak and raise the risk of a fire.
Braun Corporation · 4 vehicles
The truck has an incorrect load carrying capacity label, which could lead to improper loading of the vehicle and raise the risk of a crash.
Toyota Motor Corporation · 1 vehicles