Archive
632 recalls were announced in July 2025.
Of the 632 recalls this month scored against our rubric, 1% are Critical, 37% are Severe.
Which agencies issued them
KidKraft Farm to Table play kitchens are being recalled because clothing can catch on the accessory hooks. A 23-month-old child died from strangulation and asphyxia in February 2023.
IKEA 365+ VÄRDEFULL garlic presses are being recalled because small metal pieces can detach, posing laceration and ingestion hazards. Three lacerations have been reported globally.
The Cosco 2-Step Kitchen Stepper is being recalled because the safety bar can detach or break while in use. Thirty-four reports include two incidents resulting in head injuries.
Tegu Magnetic Floating Stackers are being recalled because magnets can loosen and detach, violating the mandatory standard for toy magnets. Thirty-one reports of magnets separating have been received.
Premier Trailer Solutions is recalling 2024 Reel and Pole trailers because improperly installed oil seals may leak oil onto the brake system, reducing braking ability.
Baby Loren Morning children's cotton loungewear dresses are being recalled because they violate the flammability standards for children's sleepwear. About 340 units are affected.
RIDGID 18Volt Brushless 21-Degree and 30-Degree Framing Nailers are being recalled because the dual action engagement system can malfunction and involuntarily discharge a nail. About 64,000 units affected.
Storyteller Overland is recalling 2023 Mode LT recreational vehicles because improperly tightened shore power inlets may overheat and cause a fire. Dealers will replace the inlets free of charge.
Amazon Basics Premium Foam Eurotop Mattresses are being recalled because they violate a mandatory flammability standard for mattresses. About 2,700 units are affected.
Leatherman Charge Plus and Charge Plus TTi multi-tools are being recalled because the tip of the knife blade does not fully fold into the handle, posing a laceration hazard. About 17,000 units affected.
SunBiotics Activated Almonds Infused with Probiotics, Oat Milk Chocolate, are being recalled after the firm detected Salmonella on one batch. 196 units are affected.
Needle Mushrooms in 200 gram packages, a product of China, are being recalled because the product tested positive for Listeria monocytogenes. 80 cases are affected.
The Medtronic CareLink SmartSync Patient Connector is being updated because in prior application versions the abort window during an induction test limited the user's ability to cancel high voltage therapy. 22,091 devices affected.
Turkeyfoot Creek Creamery Cacao Brownie Bites Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy and wheat. All expiration dates are affected.
Turkeyfoot Creek Creamery Cookies and Cream Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy and wheat. All expiration dates are affected.
Artisan Style 1/2 Loaf white bread is being recalled because product containing hazelnuts was put in bags whose allergen statement does not include hazelnuts. 883 loaves are affected.
Ritz Peanut Butter Cracker Sandwiches are being recalled because of undeclared peanut allergens due to mispackaging. 37,985 units are affected across nearly every state.
Bodor i Series laser cutting machines are being recalled because they fail to meet certain applicable federal standards at 21 CFR 1040.10(f)(1) and (f)(2). 20 units are affected.
BD COR System Software version 8.80 and above is being recalled because of a potential functionality issue supporting the Over labeling feature that could lead to possible false negative results. 7 systems affected.
Biofinity XR Toric Contact Lenses are being recalled because lens blisters may have an incomplete or leaking seal, which may render them unsterile. 397 units are affected.
Ritz Cracker Sandwiches 20 count variety packs are being recalled because of undeclared peanut allergens due to mispackaging. 13,872 cases are affected.
Ritz Peanut Butter Cracker Sandwiches in 27.6 oz 20 count cartons are being recalled because of undeclared peanut allergens due to mispackaging. 24,446 cases are affected.
GE HealthCare Discovery MR750w 3.0T MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.
Brinkley RV is recalling certain 2025 Model Z trailers because the electrical wiring may not be secured properly, which can damage the wiring and cause a short circuit.
Turkeyfoot Creek Creamery Avalanche Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy and wheat. All expiration dates are affected.
Medtronic CareLink SmartSync Device Manager is being updated because in prior application versions the abort window during an induction test limited the user's ability to cancel high voltage therapy. 22,091 devices affected.
Turkeyfoot Creek Creamery Cacao Strawberry Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy. All expiration dates are affected.
Turkeyfoot Creek Creamery Mocha Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy. All expiration dates are affected.
GE HealthCare SIGNA Architect MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.
Turkeyfoot Creek Creamery Cookie Dough Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy and wheat. All expiration dates are affected.
Endosee System Convenience Kits with IV Tube are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 475 units affected.
The Azurion 7 M20 fluoroscopic x-ray system is being recalled because of the potential for bolts connecting the gearbox to the mounting flange of the C-arm to become loose. 78 units affected.
EMPOWR Acetabular Dual Mobility Poly Bearings are being recalled because of a packaging discrepancy in which incorrect implants were packaged, discovered through a customer complaint. 20 units affected.
The Stryker StrykeFlow Disposable Suction/Irrigator with Disposable Tip is being recalled because irrigation solution may leak into the handpiece and battery pack, causing it to malfunction.
Medline IV START KIT LAB DRAW-SH convenience kits are being recalled because they contain BD ChloraPrep Clear 1 mL Applicators that may exhibit an open seal, which may breach sterility. 184 units affected.
Budesonide Inhalation Suspension 0.5 mg/2 mL is being recalled for lack of assurance of sterility after a market complaint was received for leakage and an empty ampoule. 13,680 ampoules affected.
The Covidien Nellcor Bedside SpO2 Patient Monitoring System is being recalled because alarms may not be heard or recognized, which the manufacturer links to treatment delay. 264,790 units are affected.
Medline C-SECTION PREP convenience kits are being recalled because they contain BD ChloraPrep Clear 1 mL Applicators that may exhibit an open seal, which may breach sterility. 48 units affected.
Some DIOX-602 portable x-ray systems in use in the United States do not meet the minimum source-to-skin distance requirement of 18 cm. 530 units are affected.
HSG Procedure Trays are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 171 units are affected.
Medline blood culture convenience kits are being recalled because they contain BD ChloraPrep Clear 1 mL Applicators that may exhibit an open seal, which may breach sterility. 15,700 units affected.
Biofinity Toric Multifocal Contact Lenses are being recalled because lens blisters may have an incomplete or leaking seal, which may render them unsterile. 827 units are affected.
Turkeyfoot Creek Creamery Cacao Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy. All expiration dates are affected.
Endosee System Convenience Kits are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 991 units are affected.
Epinephrine Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL vials compounded by Imprimis NJOF are being recalled because of subpotent assay results during stability testing. 6,880 vials affected.
EMPOWR Acetabular Dual Mobility Poly Bearings, catalog number 952-28-42F, are being recalled because of a packaging discrepancy in which incorrect implants were packaged. 20 units affected.
The Stryker StrykeFlow Disposable Suction/Irrigator is being recalled because irrigation solution may leak into the handpiece and battery pack, causing it to malfunction.
GE HealthCare SIGNA PET/MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.
USDA FSIS issued a public health alert for frozen tortellini that may contain undeclared soy and sesame. Consumers with allergies should not consume the product.
Ritz Peanut Butter Cracker Sandwiches in 55.2 oz 40 count cartons are being recalled because of undeclared peanut allergens due to mispackaging. 224 cases are affected.
Medline LABOR TRIAGE KIT convenience kits are being recalled because they contain BD ChloraPrep Clear 1 mL Applicators that may exhibit an open seal, which may breach sterility. 960 units affected.
Estrone RIA kits are being recalled because a specific lot of bovine serum albumin used to manufacture the coated tubes caused falsely increased assay results. 496 units are affected.
GE HealthCare SIGNA Architect AIR MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.
Turkeyfoot Creek Creamery Chocolate Peanut Butter Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy. All expiration dates are affected.
The Natus Brain Monitor Breakout Box is being recalled after two complaints that the left side labeling showed impedance for the right side. 27 units are affected.
Herbalife Nutrition Relaxation Tea is being recalled because an incorrect ingredient was received from the supplier and used in manufacturing the finished product. 5,888 units are affected.
Middle East Coast brand Tahini Dip in 6 oz tubs is being recalled because the product may be contaminated with spoilage organisms. 658 tubs are affected.
The Ellik Evacuator Adapter, Locking, model 190-NRS, is being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU. 5 units affected.
Gedney dill pickle products, including Whole Pickles and Mini Munchers Kosher Dill, are being recalled because product slated for disposal due to damage was inadvertently sold. 3,520 cases affected.
ACUVUE OASYS MAX 1-Day MULTIFOCAL contact lenses are being recalled because of defects, specifically bubbles and voids, identified during standard finished goods testing. 114,165 lenses affected.
Gedney Ghost Pepper LIL Pickles are being recalled because product slated for disposal due to product and container damage was inadvertently sold. 3,520 cases are affected.
Gedney Zinger pickle products are being recalled because product slated for disposal due to product and container damage was inadvertently sold. 3,520 cases are affected.
Clomipramine Hydrochloride Capsules USP 25 mg are being recalled after an out of specification result for an unspecified degradation product during retention sample testing at expiry. 2,724 bottles affected.
Green Silicone Seals for Accessories, reusable 0-7 FR, model CS-G7, are being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU.
Evenity (romosozumab-aqqg) injection 105 mg/1.17 mL is being recalled because of CGMP deviations involving potential temperature excursions due to transit delays. 2 pre-filled syringes affected.
The Ellik Evacuator, model 194, is being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU. 11 units are affected.
Blue Silicone Reusable Silicone Seals 6-12 FR, model CS-B612, are being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU.
A compounded Tropicamide-Proparacaine-Phenylephrine-Ketorolac sterile ophthalmic solution is being recalled because of subpotent assay results during stability testing. 2,890 vials are affected.
The Ellik Latex Bulb, model 194-2, is being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU. 48 units affected.
The Tubing for Male Connector 194, Ellik Evacuator, model 190-4, is being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU.
The Glass Body for the 194 Ellik Evacuator, model 190A, is being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU.
Bridge to Life EasiSlush is being recalled because quarterly dose audits monitoring the gamma sterilization process were not completed on time for three lots in the first quarter of 2024. 4,528 units affected.
Prolia (denosumab) injection 60 mg/mL is being recalled because of CGMP deviations involving potential temperature excursions due to transit delays. 6 pre-filled syringes are affected.
Benlysta (belimumab) for injection 400 mg/20 mL is being recalled because of CGMP deviations involving potential temperature excursions due to transit delays. 3 vials are affected.
Sushi Wasabi 5 gram ready to eat mini packs are being recalled because the individual consumer size label does not declare the ingredient Yellow 5. 1,848 cases are affected.
The Cone with Male Tubing, Non-Locking, Ellik Evacuator, model 191-NRS, is being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU.
Terran Industries is recalling 7000lb axle assemblies because incorrect suspension components may have been installed, posing a risk of axle spring failure or wheel detachment.
Mack Trucks is recalling 2026 Granite GR trucks because incompatible brake drums and steer axles may cause loss of brake function, increasing crash risk.
Ada Valley Meat Company is recalling approximately 1,065 pounds of fully cooked frozen ground beef due to possible metal contamination. The products were distributed to five states.
Kia is recalling certain 2023-2025 Telluride vehicles because the door belt molding trim can delaminate and detach from the vehicle, becoming a road hazard.
Kia is recalling certain 2023-2025 K5 vehicles because the left and right rear window trim pieces may loosen and detach, becoming a road hazard for other vehicles.
Porsche is recalling 2024-2025 Macan 4 Electric vehicles because front seat air bags may be improperly secured, potentially preventing proper deployment during a crash.
Grech Motors is recalling certain 2020-2025 Strada, Turismo and Terreno motorhomes because the retractable awning may extend unintentionally while the vehicle is moving.
Tesla is recalling certain 2026 Model Y vehicles because the horn ground wire ring terminal may be improperly secured, causing the horn to fail. An inoperable horn increases the risk of crashes.
USDA FSIS issued a public health alert for Reser's and Molly's Kitchen ham salad products containing breadcrumbs recalled for possible Listeria monocytogenes contamination.
Ford is recalling certain 2025 Lincoln Navigator, F-150, Expedition, Bronco and Ranger vehicles because the Electronic Brake Booster module may malfunction, causing a loss of power brake assist.
Mercedes-Benz is recalling certain 2022-2023 EQB 300 and EQB 350 4MATIC vehicles because the high voltage battery bus bar may be secured with incorrect screws, causing a sudden loss of drive power.
Forest River is recalling 2025-2026 Sunseeker, Solera, and other motorhomes because fuel line connectors may detach, creating a fire hazard.
BMW is recalling certain 2025 motorcycles with the optional emergency call system because a software programming error may have deactivated eCall, so first responders may not be notified of a crash.
Ford is recalling 2025 F-150 Hybrid vehicles because the seat belt warning chime may not activate. Dealers will update software to fix the issue.
Ford is recalling specific Bronco Upfit kits because the rearview camera may not display an image, increasing crash risk. Dealers will replace the camera free of charge.
Ford is recalling certain 2025 Lincoln Aviator vehicles because when using the global closing feature, the side rear windows may exert excessive force on an object before automatically reversing.
Electric Bug Zapper Racket fly and mosquito swatters, model BZ-001, are being recalled because the rechargeable battery can catch fire when used for extended periods. About 29,000 units affected.
Apollo City 2024 model year electric scooters are being recalled because the weld line can crack, causing the stem to break. Ten weld cracks have been reported and four riders came off the scooter.
Transpro A3 Hub Motor, A11F Spark and R1 Commuter electric scooters are being recalled. One scooter caught fire, causing at least $200,000 in property damage. 700 units are affected.
FENGQS F7 Pro e-bikes with batteries made on April 21, 2024 are being recalled because the lithium-ion battery can overheat and ignite. Thirteen ignitions and two fires have been reported.
Curtis International minifridges sold under the Frigidaire name are being recalled because internal electrical components can short circuit and ignite the housing. About 634,000 units are affected.
HydroTech 5/8-inch Expandable Burst-Proof Hoses made on or before August 31, 2024 are being recalled because they can burst. At least 222 bursts and 29 injuries have been reported.
Minecraft Light-Up Slap Ruler Bracelets are being recalled because the battery compartment can be opened easily by children, violating the mandatory toy standard. About 75,900 units affected.
Creekwood Naturals Gum Spirits of Turpentine bottles are being recalled because they violate the mandatory standard for child-resistant packaging. About 9,000 units are affected.
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