Recall archive
Recalls, week of May 4, 2026
36 recalls from May 4, 2026 to May 10, 2026. Urgent ones come first.
FDA Class IFDA·Medical devices Updated software is now available for the Accolade family of pacemakers and CRT pacemakers, and the advisory now covers all CRT-P and dual-chamber extended life (DR-EL) devices.
Boston Scientific Corporation · 1,404,232 units

The toys hold button batteries that children can easily get to, and a swallowed battery can cause serious injuries, including internal chemical burns, and death.
ZMC Group, Inc., of Los Angeles, California · About 124,560 units

FDA Class IFDA·Medical devices A security weakness in the Bluetooth Low Energy (BLE) communication of these battery-operated wheelchairs, found through the CISA VDP program, affects units running older software versions.
Whill, INC. · 7,009 units


The enoki mushroom product tested positive for Listeria Monocytogenes, and it was sold in 150g clear plastic packages with a black label with blue lettering.
Hemu Trading INC · 1056 cases




Do not driveNHTSA·Cars and vehicles A component missing from the drivetrain transfer case may cause the front and/or rear wheels to lock up without warning to the driver, which increases the risk of a crash.
General Motors, LLC · 66 vehicles
The lemonade contains Yellow No. 5, a color additive that is not listed on the label, which matters for anyone who needs to avoid it.
King Juice Company, Inc. · 299,779 cases
The rearview camera image may show up late when the car is put in reverse, which reduces the driver's view behind the car and raises the risk of a crash.
Tesla, Inc. · 218,868 vehicles
The power transfer unit (PTU) in certain 2019-2023 Jeep Cherokee vehicles may fail, which may cause a loss of drive power or vehicle rollaway and raise the risk of a crash or injury.
Chrysler (FCA US, LLC) · 61,711 vehicles
The non-tamperproof battery door supplied with the sound processor does not meet a safety standard because the button/coin cell battery can be replaced without using a tool.
Advanced Bionics, LLC · 45173 units
The 0.5 oz (14 g) tubes of Lidocaine Wound Gel sold under the CVS Pharmacy name failed pH specifications, meaning the gel's acidity did not meet the required standard.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Water-Jel Technologies, LLC · 31,488 tubes
A software error in the powertrain control module may let the truck go faster than its tires are rated for, which can cause a loss of vehicle control and raise the risk of a crash.
Chrysler (FCA US, LLC) · 12,736 vehicles
The popping boba contains colors that are not approved for use, namely tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6) and allura red (FD&C Red 40).
Guangdong Zonegoing Food Co., LTD · 5,196 units
Some vent fans may be missing a hinge pin, so the lid can come off and land on the road, where it could cause other drivers to crash.
Dometic Corporation · 3,094 pieces of equipment
The recalled Specially SELECTED Vanilla Creme Brulee, packaged in glass jars, may contain foreign objects, specifically glass.
Lactalis Canada, INC · 2,869 cases
A foreign object was found inside a retail container of My Mochi Strawberry flavored Non-Dairy Frozen Dessert, 7.5 oz, 6 pieces per container, UPC 0-70934-99645-8.
The Mochi Ice Cream Company, LLC · 1270 cases
With software versions 1.4.2 and 1.4.3, a delayed Dexcom G7 sensor reading can make the pump switch to non-sensor dosing, giving no correction doses or insulin cuts, which risks severe high or low blood sugar.
Beta Bionics, Inc. · 1,080 units
The cup is labeled Plain Whipped Cream Cheese Spread while the lid says Honey Almond, and the product contains almond that is not declared as an allergen.
Schreiber Foods Inc · 940 cases
The bottles hold turpentine and mineral spirits but lack the child-resistant packaging the law requires, so young children who swallow the contents could be seriously hurt or die from poisoning.
Natural Pigments LLC, of Willits, California · About 860 units

The brake lights on these RV chassis may stay lit when the driver is not braking, which can fail to show other drivers what the driver intends to do and raises the risk of a crash.
Shyft Group · 836 vehicles
The 200 gm pouches contain food colorings (Yellow 6, Blue 1 and Yellow 5) that are not listed on the label, plus Acid Red 14, a coloring that is not approved for use in food.
Ganesha Enterprises LLC · 347 pieces/ 200 gm pouch
The brake pads on these motorcycles may not work as intended on wet roads, which can lengthen the distance needed to stop and raise the risk of a crash.
Taizhou Qianxin Vehicle Co. Ltd · 216 vehicles
The propane hose may be routed over the exhaust heat shield, where heat could damage it and cause a fuel leak, which raises the risk of a fire.
Winnebago Industries, Inc. · 155 vehicles
The drawstrings on these gray youth sweatshirts can get caught on objects and could strangle a child, causing serious injury or death, and they break federal rules for children's upper outerwear.
Allura Imports Inc., of New York, New York · About 120 units

The load carrying capacity modification label on these vehicles states the wrong load carrying capacity, which may lead to improper loading of the vehicle and increase the risk of a crash.
Toyota Motor Corporation · 94 vehicles
A limited number of bottles of Alendronate Sodium Oral Solution that were stored on their side had assay test results that were out of specification.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Hikma Pharmaceuticals USA INC · 4 single dose 75 ml bottles
The FDA found manufacturing practice problems at the maker's plant during an inspection, so there is no assurance the eye drops are sterile.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Thea Pharma, Inc.
The company could not be sure these 0.33 fl oz Optase Dry Eye Intense Drops (Glycerin 0.2%) were sterile, which is the reason given for the recall.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Scope Health
Alcon cannot be sure these eye gels are sterile, because FDA inspection findings may affect the quality of the products.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Alcon Research LLC