Archive
426 recalls were announced in May 2025.
Of the 426 recalls this month scored against our rubric, 1% are Critical, 26% are Severe.
Which agencies issued them
Ford is recalling 2022-2023 Transit vehicles previously repaired under recall 22V415 because the instrument panel may fail to illuminate warning lights or gauges, increasing crash risk.
Ford is recalling 2021 F-150 trucks with Onboard Scales because a previous software update may have disabled the reverse lights, increasing crash risk.
Ford is recalling 2020 Expedition and Navigator vehicles where previous repairs left pre-collision assist features inoperative due to a software error.
Ford is recalling 2016-2017 Explorer vehicles because the driver and front passenger B-Pillar door trim may detach while driving, creating a road hazard.
Ford is recalling certain 2024 Lincoln Nautilus vehicles because multimedia module software may cause the panoramic and centre displays to reboot, leaving a blank screen.
Ford is recalling certain 2020-2023 Lincoln Aviator and Corsair vehicles with Revel Audio, previously repaired under 22V-953, because the unbelted warning chime may sound for under four seconds.
Ford is recalling 2018-2020 Expedition and Lincoln Navigator vehicles because seat belt pretensioners may lock, preventing belts from retracting or extending.
Ford is recalling certain 2023-2025 Escape, Maverick, Bronco Sport, Lincoln Nautilus and Corsair vehicles with engine block heaters because the heater may overheat when the vehicle is parked and plugged in.
Ford is recalling 2022 F-150 Lightning vehicles with specific tires to fix a software issue that prevents the tire pressure warning light from illuminating.
Rolanstar 6-Drawer Dressers sold on Amazon are unstable and pose serious tip-over and entrapment hazards to children if not anchored to the wall. About 1,293 units were sold between September 2023 and March 2025.
Nezmdi infant swings pose a suffocation risk because they exceed safe incline angles and were marketed for infant sleep. About 1,420 units sold on Amazon from September 2024 through February 2025 lack required safety warnings.
Macy's is recalling Holiday Lane Infant Footed Pajamas because the ankle elastic can be too tight, restricting blood circulation and causing injury. The company has received four reports of chafing, imprinting, or circulation restriction.
Mazda is recalling 2024-2025 MX-5 vehicles where the Dynamic Stability Control indicator light may fail to illuminate due to a software error. This could prevent drivers from being warned of a traction control system failure, increasing crash risk.
USDA FSIS issued a public health alert for Signature SELECT chicken soup cups containing undeclared wheat. Consumers with wheat allergies should not consume the products.
Sivan six-drawer double dressers can tip over without wall anchoring, posing serious injury or death risk to children. About 170 units sold on Wayfair from May 2024 to March 2025 are affected.
Shyft Group is recalling 2022-2024 Utilimaster Velocity vehicles because they may be missing the tire and information placard, which is required by federal safety standards.
Primark is recalling DTR Plush Bag Stitch and DTR Plush Bag Angel products because the zipper pull can detach, posing a choking and ingestion risk to children.
Zoox is recalling Automated Driving Systems with older software that may fail to detect people next to the vehicle, increasing injury risk.
Medical Depot Inc. is recalling 89,532 units of the iGo2 DC Car Adapter used with iGo2 Portable Oxygen Concentrator Systems. The DC power supply housing may become excessively hot to the touch and deform, posing a burn and fire hazard.
Vyaire Medical is recalling the AirLife Infant Heated Wire Circuit (Model AH165) because adapters may disconnect during setup or use, interrupting ventilation to infants and potentially causing severe complications.
Knockroe Inc is recalling Bonya Strawberry Yogurt Parfait cups (8 oz) distributed to NY, PA, MA, and NJ because they contain undeclared almonds, a common allergen.
Knockroe Inc is recalling Bonya Pineapple Yogurt Parfait (8oz cups) distributed to NY, PA, MA, and NJ because the product contains undeclared almonds, a common allergen that is not listed on the label.
Knockroe Inc is recalling Bonya Lemon Yogurt Parfait (8oz) because it contains undeclared almonds, a common allergen. The product was distributed to New York, Pennsylvania, Massachusetts, and New Jersey.
LeMaitre Vascular is recalling TufTex Over-the-Wire Embolectomy Catheters due to incomplete seals on some packages that compromise the sterile barrier. Affected units were distributed nationwide and internationally.
Knockroe Inc is recalling Bonya Black Cherry Yogurt Parfait due to undeclared almonds, which pose a risk to people with tree nut allergies. The product was distributed in NY, PA, MA, and NJ.
Ray & Mascari, Inc. is recalling tomatoes sold in retail 4-count clam shell containers and bulk cardboard cases due to potential Salmonella contamination. Affected products were distributed in IN, KY, MA, MD, MI, NC, OH, PA, and WI.
Baxter Healthcare Corporation is recalling Welch Allyn Life2000 Compressor units due to a cybersecurity vulnerability discovered during internal testing.
H&C Farms Raw Premium Tomatoes are being recalled due to potential Salmonella contamination. The recall affects tomatoes distributed to eight U.S. states.
ICU Medical is recalling LifeShield Drug Library Management software v2.1 and v2.2 due to defects that could allow over-delivery of medication to patients or unauthorized modification of drug parameters.
Empower Pharmacy is recalling Testosterone Cypionate Injection 200 mg/mL (Lot 202364, 8,230 vials) distributed nationwide because the manufacturer cannot assure the product's sterility. Consumers should stop using the product and consult their healthcare provider.
Vyaire Medical is recalling the AirLife Infant Heated Wire Circuit (model AH265) because adapters may disconnect during setup or use, potentially interrupting ventilation to newborns. Disconnection can cause hypoxia, hypercapnia, and organ failure.
Knockroe Inc is recalling Bonya Passion Fruit Yogurt Parfait (8 oz) due to undeclared almonds, which poses a risk to consumers with tree nut allergies. The product was distributed to New York, Pennsylvania, Massachusetts, and New Jersey.
Nipro Renal Solutions USA is recalling MedicaLyte Liquid Bicarbonate Concentrate (models BC+201 and BC+100) due to the potential presence of visible foreign matter in the product.
Knockroe Inc is recalling Bonya Strawberry-Banana Yogurt Parfait (8oz) because the product contains undeclared almonds, which pose a risk to consumers with tree nut allergies.
Baxter Healthcare Corporation is recalling the Welch Allyn Life2000 Ventilation system due to a cybersecurity vulnerability discovered through internal testing. The recall affects 4,881 units distributed worldwide.
Holley Performance Products is recalling specific Fuel Pressure Regulators because a damaged diaphragm may cause a fuel leak, increasing the risk of fire.
Knockroe Inc is recalling Bonya Raspberry Yogurt Parfait (8oz) because it contains undeclared almonds, which pose an allergy risk. The recall affects 6,984 units distributed to NY, PA, MA, and NJ.
Mack Trucks is recalling 2026 MD vehicles because the center bench seat belt assembly may be routed incorrectly, potentially failing to restrain occupants in a crash.
Abbott Molecular is recalling the Alinity m Resp-4-Plex AMP Kit (List Number 09N79-096) due to reports of increased reactive negative controls and false positive results in respiratory viral testing.
LeMaitre Vascular is recalling Pruitt Occlusion Catheters (catalog numbers 2103-36, 2103-46, 2103-56, E2103-36, E2103-46, E2103-56) because some packages have incomplete sterile barrier seals, potentially compromising product sterility.
Wells Enterprises is recalling Planet Smoothie ZSA Vanilla Flavored Fat Free Frozen Yogurt (3-gallon tubs) because plastic foreign material may be present in the product.
Wells Enterprises is recalling GFGB 12% Vanilla Flavored Ice Cream (3-gallon tubs) because plastic foreign material may be present in the product. Consumers should not consume the product and should contact the company or retailer.
May Flower International Inc is recalling Beijing Soybean Paste (8.82 oz/250g packages) because the product contains undeclared wheat, posing a risk to consumers with wheat allergies.
Knockroe Inc is recalling Bonya Coconut Yogurt Parfait (8 oz) distributed to NY, PA, MA, and NJ because it contains undeclared almonds, a common allergen.
Volkswagen is recalling certain 2024-2025 Atlas and Atlas Cross Sport vehicles because a software error may distort the rearview camera image when the vehicle is in reverse.
Wells Enterprises is recalling Quick Blend Vanilla Flavored Ice Cream (3-gallon tubs) because plastic material may be present in the product.
Wells Enterprises is recalling Scooper Hero Ice Cream 3-gallon tubs because plastic foreign material may be present in the product.
Wells Enterprises is recalling Vanilla Frozen Yogurt 3-gallon tubs due to the possible presence of plastic material in the product.
The Hot Chocolatier - St. Elmo, LLC is recalling Blueberry Lemon Scones sold in bulk bakery boxes because they contain undeclared soy, a common allergen.
Philips is recalling Enterprise 1.5T MRI scanners (Model 781145) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
LeMaitre Vascular is recalling Pruitt Irrigation Occlusion Catheters (Catalog Numbers 2102-09, E2102-09) due to incomplete sterile barrier seals found during internal testing. The defect affects approximately 26,872 units distributed nationwide and internationally.
Abbott Molecular is recalling the Alinity m Resp-4-Plex Amplification Kit due to reports of reactive negative controls and false positive results in respiratory virus testing.
Dixit Foods Pohe (110 g packages) is recalled due to undeclared milk and/or peanut allergens. The product was distributed in California, Utah, and Washington.
Knockroe Inc is recalling Bonya Blueberry Yogurt Parfait (8 oz) distributed in NY, PA, MA, and NJ because the product contains undeclared almonds, which poses a risk to consumers with tree nut allergies.
Wells Enterprises, Inc. is recalling Ellington Farms Vanilla Flavored Ice Cream (3-gallon tubs) distributed across the US because plastic material may be present in the product.
Knockroe Inc is recalling Bonya Peach Yogurt Parfait (8oz cups) distributed to NY, PA, MA, and NJ due to undeclared almonds that may pose a risk to consumers with tree nut allergies.
Knockroe Inc is recalling Bonya Mango Yogurt Parfait (8oz) because it contains undeclared almonds, a major food allergen. The product was distributed to NY, PA, MA, and NJ.
Klinika Medical is recalling the KliniTray tissue resection margin examination board (Model 2001105-F) due to potential microbial contamination. The device was distributed nationwide in Massachusetts.
Dixit Foods Sabudana Khichadi (200 g) is recalled due to undeclared milk and/or peanut allergens. The product may pose a serious risk to consumers with allergies to these ingredients.
Cook Incorporated is recalling Tornado Embolization Microcoils due to incorrectly sized coils in affected lots. The devices are used for vascular embolization procedures.
New England Village Snacks The 19th Hole Snack Mix (5 oz. and 10 oz.) is being recalled due to undeclared almonds and sesame. Consumers with allergies to these ingredients should not consume the product.
Knockroe Inc is recalling Bonya Vanilla Yogurt Parfait (8oz) due to undeclared almonds, which pose a risk to consumers with almond allergies. The product was distributed to NY, PA, MA, and NJ.
Advance Food International Inc. is recalling Kasundi Peeled Mango Pickle in Oil due to elevated lead levels detected in the product. The affected product was distributed in the Northeast.
Philips is recalling Intera 1.5T Explorer/Nova Dual MRI scanners (Model 781108) due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges that could contact patients during scanning and cause skin injuries.
Philips is recalling Intera 1.5T MRI systems due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges and contact patient skin during scanning.
Philips is recalling the Intera 0.5T Standard MRI system (Model 781101) because the Quadrature Body Coil seal adhesive may fail and create sharp edges that could injure patients during scanning.
Wells Enterprises is recalling Peanut Butter 'N Fudge Ice Cream 3-gallon tubs because plastic foreign material may be present in the product.
Philips is recalling 103 Intera 1.5T MRI scanners worldwide because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could cause skin abrasions, bruises, lacerations, hair loss, or tissue injury to patients.
Philips is recalling SmartPath to dStream 3.0T MRI systems (Model 782145) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Medline Industries is recalling Centurion Sterile Weitlaner Retractor 3 x 4 Prong units because the retractors may puncture through the sterile packaging. The product is distributed nationwide.
Philips is recalling SmartPath to dStream 1.5T MRI units (Model 782146) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could cause skin abrasions, lacerations, or tissue injury to patients.
Wells Enterprises is recalling Glenview Farms Chocolate Ice Cream 3-gallon tubs due to possible plastic foreign material in the product. The affected ice cream was distributed to 103 distribution centers across the United States.
Philips is recalling the Intera 1.5T Omni/Stellar MRI scanner due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges and cause patient injury. The loose seal during scanning could result in skin abrasions, bruises, lacerations, hair loss, or tissue damage.
KliniTray Platte Faxitron sterile tissue resection margin examination boards (Model 2001155-F) are being recalled due to potential for microbial contamination. Affected units were distributed nationwide.
Chrysler is recalling certain 2022-2025 Ram ProMaster vehicles because a software error in the security gateway module may prevent the rearview camera image displaying, failing FMVSS 111.
Philips is recalling Intera 1.5T R11 MRI systems because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could contact patients and cause skin injuries.
Philips is recalling the Intera 3.0T Quasar Dual MRI scanner (Model 781150) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Philips is recalling Intera 1.0T Omni/Stellar MRI systems (37 units: 3 in US, 34 internationally) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that can cause skin injuries during patient scanning.
East CK Trading Inc. is recalling President Brand Kumquat Slices because they contain undeclared sulfites. Sulfites are a known allergen that can cause serious reactions in sensitive individuals.
Philips is recalling Intera CV MRI units (Model 781107) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning, including skin abrasions, lacerations, or tissue damage.
Philips is recalling the Intera 1.5T Power/Pulsar MRI scanner because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Philips is recalling Intera 1.0T Power/Pulsar MRI systems (Model 781103) due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges and injure patients during scanning.
AVID Medical is recalling Halyard RAPIDES E-PACK Cardiovascular Procedure Convenience Kits due to a raw material defect in surgical needle coating that may cause diminished performance or coating removal during use.
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.
Wells Enterprises is recalling GFGB Vanilla Bean Flavored Ice Cream in 3-gallon tubs because plastic material may be present in the product.
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 Vanilla Bean Ice Cream (3-gallon tubs) distributed by US Foods because plastic material may be present in the product.
Wells Enterprises is recalling Cotton Candy Flavored Ice Cream 3-gallon tubs because foreign plastic material may be present in the product.
Wells Enterprises is recalling Rocky Road Flavored Ice Cream 3-gallon tubs due to possible plastic material in the product. The affected ice cream was distributed to over 100 distribution centers across the United States.
Wells Enterprises is recalling Johnny Rockets Vanilla Flavored Ice Cream (3-gallon tubs) because plastic material may be present in the product.
Wells Enterprises is recalling Keith Valley Vanilla Flavored Ice Cream 3-gallon tubs due to the possible presence of plastic foreign material in the product.
Wells Enterprises is recalling Country Rich Vanilla Ice Cream 3-gallon tubs because plastic foreign material may be present in the product.
AVID Medical is recalling Halyard SUTURE PACK CABG Cardiovascular Procedure Convenience Kits due to a raw material defect in the surgical needle coating that may reduce needle performance or cause coating removal during use.
Richard Wolf GmbH is recalling 31 PiezoWave 2 Control Units (Product Number 100506US) due to a high voltage capacitor that may fail early in the device's life cycle, potentially producing smoke, burning smell, spark, or excessive heat.
Medline Industries is recalling Centurion Sterile Weitlaner Retractors (2,100 units) due to potential puncture damage to sterile packaging. The defect could compromise the sterility of the surgical instrument.
Meddev Corp is recalling Contour Gold Eyelid Weight implants (Model LL3012) due to mislabeling. Thirty-four weights distributed nationwide are affected.
AVID Medical is recalling Halyard CHRIST SUTURE KIT units due to a raw material issue in the needle coating that may cause silicone to be removed during use, potentially affecting surgical performance.
Foundation Medicine is recalling four FoundationOne Companion Diagnostic (F1CDx) test reports sent to customers that contained clinically relevant variants requiring amendment, including one with an incorrect negative companion diagnostic claim.
La Roche-Posay Effaclar Duo acne treatment is being recalled due to detected trace levels of benzene. The recall affects 2,226,801 units distributed nationwide.
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.
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