Archive
426 recalls were announced in May 2025.
Of the 426 recalls this month scored against our rubric, 1% are Critical, 29% are Severe.
Which agencies issued them
Wells Enterprises is recalling 17 3-gallon tubs of Artificially Flavored French Vanilla Ice Cream distributed by Sysco Corporation because plastic material may be present in the product.
Gordon Choice Vanilla Flavored Ice Cream in 3-gallon tubs is being recalled because plastic material may be present in the product. The affected ice cream was distributed to 103 distribution centers across the US.
Wells Enterprises is recalling Cotton Candy Flavored Ice Cream 3-gallon tubs because foreign plastic material may be present in the product.
Meddev Corp is recalling Contour Gold Eyelid Weight implants (Model LL3010, 1.0 gm) due to mislabeling. The recall affects 34 units distributed nationwide across 17 states.
Glenview Farms Artificially Flavored French Vanilla Ice Cream in 3-gallon tubs is being recalled because plastic material may be present in the product. Consumers should not consume the product.
Wells Enterprises is recalling GFGB Vanilla Bean Flavored Ice Cream in 3-gallon tubs because plastic material may be present in the product.
L'Oreal USA is recalling La Roche-Posay Effaclar 3-Step Acne Routine Kits nationwide due to trace levels of benzene detected in one lot. As a precaution, all Effaclar Duo Dual Action Acne Treatment lots are included in the recall.
Wells Enterprises is recalling Mocha Almond Fudge Ice Cream (3-gallon tubs) because plastic fragments may be present in the product. Consumers should not consume the affected product.
Wells Enterprises is recalling 3-gallon tubs of vanilla flavored ice cream due to the possible presence of plastic foreign material in the product.
Wells Enterprises is recalling Vanilla Bean Ice Cream (3-gallon tubs) distributed by US Foods because plastic material may be present in the product.
Snack Mania Brazilian Delights Corp. is recalling approximately 9,722 pounds of frozen chicken coxinhas produced without federal inspection. No illnesses have been reported.
Bourgeois Smokehouse is recalling approximately 100 pounds of ready-to-eat smoked andouille sausage sold in Alabama, Louisiana, and Mississippi due to possible Listeria monocytogenes contamination.
Braun Industries is recalling specific Demers ambulance models because improperly installed cushion equipment storage may allow items to detach during transit, increasing injury risk.
Orange EV is recalling specific electric trucks because a pintle hook blocks the backup lights, reducing visibility and increasing crash risk.
Michelin is recalling specific Agilis Cross Climate tires because chunks of tread rubber may detach, increasing the risk of tire failure and a crash.
BorgWarner is recalling traction batteries where loose hardware may detach, causing short circuits, drive power loss, and fire risks.
Isuzu is recalling 2025 NRR EV vehicles because a gap in the electrical system may cause overheating and loss of drive power, increasing crash risk.
Fijian Import & Export Co. Inc. is recalling approximately 127 pounds of ready-to-eat meat pie products imported from Australia that were not presented for FSIS import reinspection. The products were shipped to Rutter's convenience stores in Pennsylvania.
FidgetThings is recalling Chill Pill Magnetic Haptic Fidget Toys Red Bumpy because they violate federal magnet regulations and pose a risk of serious injury or death if swallowed by children.
Volkswagen is recalling certain 2025 ID. Buzz vehicles because the third-row bench is wide enough for three passengers but is designed for two and has only two seat belts, failing FMVSS 208.
Fat Brain Toy Co. is recalling PlayTab Rollers Tile Toys because they contain magnets that can become loose and be swallowed by children, posing a risk of serious injury or death.
NICREW 15" Submersible RGB LED Lights with remote controls are recalled because the remote's lithium coin battery can be easily accessed by children, creating a serious ingestion hazard that can cause internal burns and death.
Multiple child safety gates sold on Amazon.com violate federal safety regulations, posing risk of serious injury or death from entrapment and falls. Consumers should stop using the gates immediately and contact the seller for disposal and refund.
Leon Rading Co. Ltd. is recalling digital wall clocks (model PH-05) sold on Amazon because the remote control contains a lithium coin battery that children can easily access and swallow, risking serious internal injury or death.
Boyro Baby Convertible High Chairs sold on Amazon.com pose a risk of serious injury or death from falls and entrapment. The restraint system is not properly attached and can fail, and the opening between seat and tray is large enough for a child to become trapped.
LivingCaring Adult Portable Bed Rails pose a serious risk of entrapment and asphyxiation due to violations of federal safety regulations. About 280 units sold online May 2024–March 2025 are affected; consumers should stop using them immediately.
International is recalling certain 2025-2026 IC Bus CESB school buses because the parking brake can be released while the wheelchair platform lift is deployed, failing FMVSS 403.
Polaris is recalling about 640 Model Year 2023–2025 Ranger XP 1000 NorthStar and NorthStar Crew off-road vehicles because seat belt anchor fasteners may not be properly tightened, risking seat belt separation in a crash and potential ejection of riders.
Keystone RV Company is recalling specific 2024-2025 travel trailers because step mounting bolts may loosen, allowing steps to detach and increase injury risk.
KTM is recalling about 19,310 GASGAS and Husqvarna off-road motorcycles from model years 2022–2025 because the front brake caliper can crack, reducing braking effectiveness and creating a crash risk. No injuries have been reported.
Toyota is recalling certain 2022-2025 Tundra and Tundra Hybrid vehicles because moisture may enter the reverse light assemblies and cause the lights to fail.
BuddyLove is recalling about 940 children's Mini Danica loungewear sets (sizes 3–12) sold from October 2023 through July 2024 because they violate federal flammability standards for children's sleepwear, posing a burn hazard and risk of serious injury or death.
Smiths Medical is recalling CADD Solis HSPCA Pumps with wireless connection modules that may experience intermittent connection alarms, interrupting active infusions and risking serious patient injury or death.
Smiths Medical is recalling CADD-Solis VIP Ambulatory Infusion Pumps due to false Upstream Occlusion Alarms that may interrupt medication infusions, risking serious patient injury or death.
Smiths Medical is recalling CADD-Solis and CADD-Solis VIP ambulatory infusion pumps because they may trigger a false upstream occlusion alarm that interrupts therapy, risking serious patient injury or death.
BRS Analytical Services is recalling Lubricant Eye Drops Solution (Polyethylene Glycol 400 and Propylene Glycol) due to manufacturing deviations and lack of assurance of sterility. The product was distributed nationwide.
Ankimo branded Monkfish Liver (7 oz) is recalled because it contains undeclared milk, a common allergen. Consumers with milk allergies should not consume this product.
Optimal Carnivore, LLC is recalling Bone & Joint Restore capsules nationwide due to potential contamination with salmonella. Consumers should stop using the product and contact the manufacturer.
BRS Analytical Services is recalling Artificial Tears ophthalmic solution (0.5 FL OZ dropper bottles) nationwide due to manufacturing deviations and lack of assured sterility. Affected lots are Lot 126–129, 162–170, and 193–199.
Smiths Medical is recalling CADD Solis VIP Ambulatory Infusion Pumps due to potential thermal damage. The recall affects 313,676 units distributed nationwide and worldwide.
Integra LifeSciences is recalling CODMAN Craniotomy Kits due to inadequate welds that may cause the product to disassemble. The defect affects 1,840 units distributed worldwide.
Smiths Medical is recalling CADD-Solis infusion pumps worldwide due to a potential for thermal damage. The affected pumps include multiple models and variants distributed in the US and internationally.
Taylor Farms Illinois Inc. is recalling Trader Joe's Sesame Miso Salad with Salmon (10.25 oz.) because it contains undeclared milk, which poses a risk to consumers with milk allergies.
BSO LLC is recalling Testosterone Pellet 200 mg compounded drug vials nationwide due to the presence of glass particles found in pellet vials.
Bausch & Lomb is recalling enVista Envy and enVista Envy Toric intraocular lenses due to increased reports of toxic anterior segment syndrome (TASS) following implantation.
Integra LifeSciences is recalling CODMAN Disposable Perforators (14mm) due to inadequate welds that could cause disassembly during use. The affected devices have been distributed worldwide.
Bausch & Lomb has recalled multiple enVista intraocular lens models used in cataract surgery due to reports of toxic anterior segment syndrome (TASS) in the United States. TASS is an inflammatory reaction in the front of the eye following lens implantation.
Amneal Pharmaceuticals is recalling Ropivacaine Hydrochloride Injection 0.5% due to the presence of particulate matter. The recall affects specific lots distributed nationwide.
Apollo Care, LLC is recalling FentaNYL 500mcg/2mcg/mL and Ropivacaine HCl 250mg/0.1% epidural injection due to lack of assurance of sterility. The recall affects 440 bags of a single lot distributed in Missouri.
BRS Analytical Services is recalling Polyvinyl Alcohol Ophthalmic Solution 1.4% eye drops nationwide due to cGMP deviations and lack of assurance of sterility.
Trophy Nut Company is recalling Heinen's Honey Roasted Peanuts because the product is labeled as containing only peanuts but may contain undeclared cashews, a tree nut allergen.
BRS Analytical Services is recalling Carboxymethylcellulose Sodium Ophthalmic Gel 1% eye lubricant due to current Good Manufacturing Practice (cGMP) deviations and lack of assurance of sterility.
BSO LLC is recalling Testosterone Pellet 200 mg compounded drug vials nationwide because glass particles were found in the pellets intended for subcutaneous injection.
BSO LLC is recalling compounded testosterone pellets nationwide because glass particles were found in vials. Affected lot numbers are 20250207@1 and 20250228@1 (expiration 1/31/2026).
BRS Analytical Services is recalling Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% eye lubricant nationwide due to cGMP deviations and lack of assurance of sterility. The recalled product was distributed in 0.5 FL OZ dropper bottles across multiple lots with various expiration dates in 2025 and 2026.
Galt Medical Corporation is recalling certain Introducer Kit–Coaxial Dilator models due to potential open seals in sterile barrier packaging, which could compromise sterility.
Galt Medical Corporation is recalling the B Braun Interventional ELITE HV Hemostasis Valve Introducer System (Catalog Number 612802, Model BCL-100-04, Lot S25128171) due to a potential open seal in the sterile barrier packaging. The defect may compromise the sterility of the device.
BSO LLC is recalling Testosterone Pellet 200 mg vials nationwide due to the presence of glass particles found in pellet vials. Patients should contact their healthcare provider.
Lamb Weston Inc is recalling approximately 3,789 cases of frozen hashbrown patties due to the presence of plastic pieces measuring 1–8 mm in the product. No illnesses have been reported.
Philips is recalling Microstream Advance Neonatal-Infant Intubated CO2 Filter Lines and related products because the adapter may be difficult or impossible to disconnect from the endotracheal tube.
WANDERCRAFT SAS is recalling the Atalante X powered exoskeleton due to a potential loss of lateral balance that could cause patients to fall. Three units have been distributed to rehabilitation facilities in Pennsylvania and New York.
Galt Medical Corporation is recalling 2,881 GALT Centeze Catheters due to a potential open seal in the sterile barrier packaging. The open seal could compromise sterility of the device.
Galt Medical Corporation is recalling Introducer Kit-Tearaway MicroSlide devices used to introduce catheters into blood vessels due to a potential open seal in the sterile barrier packaging. The affected units may not maintain sterility, creating a risk of infection.
Inari Medical is recalling 45 units of the Artix MT Thrombectomy Device (REF: 32-102, Lot 24100082) because labeling specifies an incorrect vessel range of 2.5-6 mm instead of 3-6 mm, which could increase radial force on arteries and cause vascular complications.
Ford is recalling certain 2022-2023 Bronco vehicles because the 360-degree view camera may not display a rearview image when the vehicle is placed in reverse.
Galt Medical Corporation recalls Introducer Needle REF NDL-107-04 due to potential open seals in sterile barrier packaging, which could compromise product sterility.
Lamb Weston Item M7414 frozen hashbrown patties are recalled because approximately 1mm to 8mm pieces of plastic were found in the product. The affected cases were distributed in Arizona, Hawaii, and internationally.
Winnebago is recalling 2023-2024 Commercial Vehicles because step mounting bolts may loosen, allowing steps to detach and increasing the risk of injury.
Remote Diagnostic Technologies Ltd. is issuing a software update for the Philips Tempus Pro Patient Monitor due to freezing, rebooting, and potential ECG measurement accuracy issues across multiple software versions.
Getinge Disinfection Ab is recalling Washer Disinfector Aquadis 56 (Model 56A) units due to a frequency inverter programming error that causes the circulation pump to start earlier than expected, leading to accelerated wear on the axial seal.
One lot of Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits (Model 750830) was stored at improper temperatures in Medline warehouses. The test kits may not perform as intended due to storage outside labeled requirements.
FDC Limited is recalling Timolol Maleate Ophthalmic Solution 0.5% due to a defective container where the spike of the cap becomes lodged in the bottle nozzle, preventing users from accessing the solution.
Philips is recalling IntelliSpace Cardiovascular software versions 6.x, 7.x, and 8.x because the Echo Module may generate reports with missing or incomplete information.
Ambu Inc. is recalling 160 units of the Ambu aScope 5 Broncho HD 5.6/2.8 Sampler Set due to incorrect front pouch labeling that states 5.0/2.2 instead of the correct size 5.6/2.8.
BSO LLC is recalling Testosterone Pellet 100 mg (compounded, office use only) distributed nationwide due to glass particles found in pellet vials.
Galt Medical Corporation is recalling B Braun Interventional Coaxial Dilator Micro-Introducer Kits due to a potential open seal in the sterile barrier packaging. The affected kits are distributed nationwide in eight U.S. states and six countries.
Galt Medical Corporation is recalling GALT Guidewire model SGW-051-07 due to a potential open seal in the sterile barrier packaging. The defect may compromise the sterility of the device.
RemedyRePack Inc. is recalling Clindamycin HCl Capsule, 300 mg, due to current Good Manufacturing Practice (CGMP) deviations—the products were manufactured in a shared facility with Ezetimibe tablets.
Siddha Flower Essences is voluntarily recalling Temper Tamer homeopathic oral spray due to Current Good Manufacturing Practice (CGMP) deviations identified during manufacturing.
Lamb Weston frozen hashbrown patties may contain pieces of plastic material measuring 1–8 mm. The affected product was distributed in Arizona, Hawaii, and several international locations.
Lamb Weston Inc is recalling frozen foodservice hashbrown patties due to plastic pieces (1–8 mm) found in the product. Affected cases were distributed to Arizona, Hawaii, Japan, Kuwait, Taiwan, and UAE.
Bio 1 Granules for Filling implant bone granules may contain less product than specified on the label. The affected lot is 240781 (UDI: 03760154000369), distributed nationwide.
Tornier's Blueprint Software version 4.2.1 contains a bug that prevents surgeons from accessing surgical cases created in earlier software versions.
Integra LifeSciences is recalling INSPIRA AIR Balloon Dilation System 10x40 cartons because an incorrect product was packaged inside. The recall affects six units distributed across Texas, Montana, Alabama, and Oklahoma.
Getinge Disinfection Ab recalls the Washer Disinfector Aquadis 56 (Model 56M) because the frequency inverter is not programmed to specification, causing the circulation pump to start earlier than expected and wear the axial seal prematurely.
Mitsubishi Fuso is recalling 243 2024 Rizon trucks because a defective bulb socket may cause front turn signals to burn out, increasing crash risk.
USDA FSIS issued a public health alert for Rachael's Food Corporation chicken and bacon ranch wraps due to possible Listeria monocytogenes contamination. No recall was requested as products are no longer available for purchase.
Mercedes-Benz is recalling 443 vehicles that received an incorrect fuse box during a previous recall. The defect may cause loss of drive power, safety functions, or fire.
ATC is recalling 2025 PLA550 Bumper Pull trailers because the power wire to stabilizer jacks may lack over-current protection, increasing fire risk.
Waymo is recalling 5th Generation Automated Driving Systems with older software that may cause vehicles to collide with roadway barriers like chains and gates.
Ford is recalling certain 2024-2025 Bronco and Ranger vehicles because the front upper control arm ball joint fastener may be missing or improperly tightened.
Ford is recalling certain 2022-2024 Expedition and Lincoln Navigator vehicles because front brake lines may contact the engine air cleaner outlet pipe and leak brake fluid.
Ford is recalling certain 2025 Explorer and Lincoln Aviator vehicles because a mounting bolt for the front subframe may have been tightened improperly. 206 units affected.
Ford is recalling 2025 F-150 vehicles because lower steering shaft fasteners may detach, causing loss of steering control and increasing crash risk.
Ford is recalling certain 2024-2025 Bronco vehicles because front lower control arm fasteners may not be tightened, allowing the arm to detach. Owners are told not to drive.
Forest River is recalling 2025 Cherokee ACKT271RK travel trailers because they may lack an emergency exit window, which could delay evacuation during an emergency.
Ford is recalling certain 2024 Bronco vehicles because the left-side rear door may be opened from inside the vehicle when the child safety lock is in the ON position.
Ford is recalling certain 2021-2022 Bronco vehicles repaired incorrectly under recall 22V-825, because the rearview camera image may still display after backing has ended.
Ford is recalling a wide range of 2021-2025 vehicles because a software error may cause the rearview camera image to freeze or go missing. 1,076,138 units are affected.
Ford is recalling 2022-2023 F-150 Lightning vehicles previously repaired under recall 23V801 because software may fail to activate electronic stability control, increasing crash risk.
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