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
Ford is recalling certain 2021–2023 Ford and Lincoln vehicles because the low-pressure fuel pump may fail, causing engine stalls while driving and increasing crash risk.
Polestar is recalling certain 2025 Polestar 3 vehicles because water may damage electrical connectors between the engine bay and front bumper, which can cause loss of power steering assist and increase crash risk.
Jaguar Land Rover is recalling 2020–2025 Range Rover Evoque vehicles because the passenger air bag may tear during deployment, reducing occupant protection and risking burn injury from escaping gases.
Shyft Group is recalling 2015-2025 Utilimaster Truck Body vehicles because a signal converter failure can cause brake lights and turn signals to stop working.
Jeriflyer 8-inch pool drain covers sold on Amazon do not meet federal safety standards and pose a risk of serious injury or death from entrapment. Consumers should immediately stop using affected pools and contact the seller for a refund.
DEWALT has recalled approximately 17,680 Elite Series 40G T27 High Density Flap Discs because the ceramic cloth abrasive flaps can detach during use, causing laceration and injury. Three reports of the flaps detaching resulted in cuts and scrapes.
509 helmets and 509 for Polaris helmets may fail to provide sufficient protection in a crash. One incident reported a helmet detachment during a crash resulting in a concussion.
SNLN Party Supply Toys containing button cell batteries are being recalled because the battery compartments can be easily opened by children, posing a risk of serious injury or death if swallowed.
Trane U.S. Inc. recalls about 4,790 Gas/Electric Packaged Units because the fuel gas valve can open unexpectedly, causing a gas leak and fire hazard. No injuries have been reported.
Positec is recalling about 49,000 Hyper Tough, Worx, and Portland brand electric corded chainsaws and pole saws due to a defective main switch that can fail and allow the saws to continue running, posing a laceration hazard.
Autocar is recalling certain 2015-2022 Xspotter and Xpeditor vehicles with insufficient air in their brake system tanks. The defect can reduce brake function and increase stopping distance.
Harbor Freight Tools is recalling about 6,500 Predator 2000-Watt Power Stations due to reversed wires in the AC outlet receptacles when in Emergency Power Supply mode, creating a shock hazard to consumers.
NHTSA is recalling 2025 Can-Am Canyon motorcycles because a drive belt support may fail, causing loss of power and increasing crash risk.
Autocar is recalling 2012-2025 Xspotter vehicles because incorrect tire inflation labels may lead to under-inflated tires, increasing crash risk.
Kraft Heinz is recalling Oscar Mayer Turkey Bacon products nationwide due to possible Listeria monocytogenes contamination. No illnesses have been reported.
Thrive Health Solutions is recalling Tirzepatide/Cyanocobalamin Injectable 15mg/1mg/mL pre-filled syringes (Lot C03065F) due to lack of assurance of sterility. The product was distributed nationwide in the USA.
Shyft Group is recalling 2024-2025 Blue ARC BA4L-800 vehicles because a brake caliper spacer may be too big, preventing the parking brake from engaging properly.
Insulet Corporation is recalling the Omnipod 5 iOS App due to a software issue where decimal separators are not recognized in manual insulin entry, potentially causing insulin overdose and severe hypoglycemia.
Hy-Vee is recalling Crunchy Shrimp Roll due to potential contamination with Listeria monocytogenes. The affected product was distributed to retail locations throughout the Midwest.
Homegrown Family Foods LLC is recalling Shore Lunch Breading & Batter Mix Oven Style because it contains undeclared milk, a common allergen. The product was distributed across multiple Midwestern and East Coast states.
Thrive Health Solutions is recalling LX Bioboost Plus pre-filled syringes due to lack of assurance of sterility. The affected product is a multi-ingredient injectable formulation distributed nationwide.
Isabelle's Kitchen, Inc. is recalling Maple Avenue Foods Crunchy Wheatberry Salad due to Salmonella contamination. The 5 lb. containers were distributed to Pennsylvania and Maryland.
Fresenius Medical Care is recalling 0.9% Sodium Chloride Injection in flexible plastic containers nationwide due to lack of assurance of sterility. The FDA classified this as a Class II recall.
Thrive Health and Wellness, LLC is recalling LL Bioboost Injectable pre-filled syringes nationwide due to lack of assurance of sterility. The affected product is Lot #H277639 with expiration 6/25/2025.
Apotex Corp. is recalling Ketorolac Tromethamine Ophthalmic Solution 0.5% due to lack of assurance of sterility. The recall affects 87,840 bottles distributed nationwide.
Hy-Vee is recalling Duo Crunchy Veg Shrimp 10Pc due to potential contamination with Listeria monocytogenes. The affected product was distributed to retail locations throughout the Midwest.
Teva Pharmaceuticals USA, Inc. is recalling Metoclopramide Tablets, USP 10 mg due to the presence of foreign tablets or capsules in the product. The affected lot is distributed nationwide.
Hy-Vee is recalling Spicy Shrimp Poke Bowl products due to potential contamination with Listeria monocytogenes. The product has been distributed to retail locations throughout the Midwest.
B Braun Medical Inc. is recalling 187,656 containers of 0.9% Sodium Chloride Injection USP due to potential sterility failures caused by pinholes in finger boxes during manufacturing. The defect may allow leaks and compromise the sterile nature of the intravenous medication.
SunMed Holdings is recalling Broselow Pediatric Emergency Rainbow Tape due to incorrect values printed on the tape that could lead to improper medication dosing and defibrillation in pediatric emergency care.
Thrive Health Solutions is recalling Tirzepatide Injections 30mg/mL pre-filled syringes due to lack of assurance of sterility. The affected product was distributed nationwide.
Advanced Pharmaceutical Technology, Inc. is recalling TESTO-200 (Testosterone Cypionate Injection USP, 200mg/ml) because it was marketed without an approved NDA or ANDA.
P East Trading Corp is recalling Salted Smoked Split Herring due to potential Clostridium botulinum contamination in uneviscerated fish. The product was distributed to retail locations in New York, New Jersey, and Connecticut.
Thrive Health Solutions is recalling Semaglutide/Cyanocobalamin Injectable pre-filled syringes due to lack of assurance of sterility. The affected lot was distributed nationwide.
Becton Dickinson is recalling BD BACTEC MGIT 960 PZA Kit due to reports of intermittent false resistance results during pyrazinamide susceptibility testing of Mycobacterium tuberculosis. The issue affects units distributed worldwide.
Thrive Health Solutions is recalling Semaglutide 5 mg/mL pre-filled syringes distributed nationwide because the manufacturer cannot assure the product's sterility.
Thrive Health Solutions is recalling one lot of Tirzepatide/Cyanocobalamin Injectable pre-filled syringes due to lack of assurance of sterility. The affected product is Lot C03125A distributed nationwide.
Target Corporation is recalling Grilled Chicken Greek Style Salad with Balsamic Dressing because the cucumber may be contaminated with Salmonella. The recall affects 220 units distributed in Illinois, Indiana, Tennessee, and Virginia.
Integra LifeSciences is recalling Extended Tip Applicator 8CM devices due to potentially out-of-specification endotoxin levels and lack of sterility assurance. The recall affects 6,216 units distributed across the US and internationally.
Integra LifeSciences Corp. is recalling the MicroMyst Applicator Box of 5 due to lack of sterility assurance. The product is used with the Integra Flow Source for controlled application of two liquids.
Integra LifeSciences is recalling Extended Tip Applicators (15 CM, Box of 5) because they may contain out-of-specification levels of endotoxins and lack sterility assurance.
Hy-Vee is recalling Red Dragon Roll products due to potential contamination with Listeria monocytogenes. The recall affects 122.5 cases distributed to retail locations throughout the Midwest.
TRI-UNION FROZEN PRODUCTS INC (Chicken of the Sea Frozen Food) is recalling frozen raw peeled and deveined tail-on shrimp because they contain undeclared sulfites, a potential allergen.
Hy-Vee is recalling Duo Crunchy Calif Shrimp 10Pc due to potential contamination with Listeria monocytogenes. Affected products were distributed to retail locations throughout the Midwest.
Hy-Vee is recalling Duo Spicy Veg Shrimp 10Pc due to potential contamination with Listeria monocytogenes. Affected product was distributed to retail locations throughout the Midwest.
Isabelle's Kitchen, Inc. is recalling Maple Avenue Foods Quinoa Tabouli Salad due to Salmonella contamination. The product was distributed to Pennsylvania and Maryland.
Mightylicious Inc. is recalling MIGHTYLICIOUS Vegan Oatmeal Coconut Cookies because they contain undeclared milk, a common allergen not listed on the label. The product was distributed to Rhode Island, Illinois, and New York.
Hy-Vee is recalling Duo Crispy Calif Shrimp 10Pc due to potential contamination with Listeria monocytogenes. Affected cases were distributed to retail locations throughout the Midwest.
Isabelle's Kitchen, Inc. is recalling Mediterranean Pasta Salad due to Salmonella contamination. The affected product was distributed in Pennsylvania and Maryland.
Hy-Vee is recalling Rock N Roll Shrimp 10Ct due to potential contamination with Listeria monocytogenes. The product was distributed to retail locations throughout the Midwest.
Isabelle's Kitchen, Inc. is recalling Greek Pasta Salad in 4.5 lb. containers due to Salmonella contamination. The recalled products were distributed to Pennsylvania and Maryland.
Isabelle's Kitchen, Inc. is recalling Maple Avenue Foods Powerhouse Wheatberry Salad Kit due to Salmonella contamination. The product was distributed to Pennsylvania and Maryland.
Hy-Vee is recalling Duo Spicy Calif Shrimp 10Pc due to potential contamination with Listeria monocytogenes. Affected product was distributed to retail locations throughout the Midwest.
Hy-Vee is recalling Crispy Shrimp Roll 10Pc due to potential Listeria monocytogenes contamination. Consumers should not consume the product.
Hy-Vee is recalling Duo Crispy Veg Shrimp 10Pc products due to potential contamination with Listeria monocytogenes. The affected products were distributed to retail locations throughout the Midwest.
Bornstein Seafoods Inc. is recalling frozen shrimp meat products after Listeria monocytogenes was detected during the firm's routine testing. The products were distributed nationwide and in Canada.
Thrive Health Solutions is recalling Methylcobalamin Injectable 10mg/mL pre-filled syringes (Lot #H228307, expiration 12/27/2025) due to lack of assurance of sterility. The affected product was distributed nationwide.
Thrive Health Solutions is recalling NAD+ 100mg/mL pre-filled syringes (Lot #O-O8A01-25) distributed nationwide due to lack of assurance of sterility. Consumers should not use this product.
Thrive Health Solutions is recalling Tirzepatide Injections (10mg/mL, pre-filled syringes) distributed nationwide due to lack of assurance of sterility. Consumers should not use the affected product and contact their healthcare provider.
Apotex Corp. is recalling Azelastine Hydrochloride Ophthalmic Solution, USP 0.05% due to lack of assurance of sterility. The affected batch was distributed nationwide.
Thrive Health Solutions is recalling Semaglutide 2.5 mg/mL pre-filled syringes (Lot #H270221) because the manufacturer cannot assure sterility of the product.
Thrive Health Solutions is recalling CJC-1295 Injectable 6mg/15mg pre-filled syringes due to lack of assurance of sterility. The affected product was distributed nationwide.
Integra LifeSciences is recalling Extended Tip Applicator 8CM devices nationwide and internationally because they may contain potentially out-of-specification endotoxin levels and lack sterility assurance.
Apotex Corp. is recalling 6,288 bottles of Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution nationwide due to lack of assurance of sterility. The affected batch (VC6058, expiration date 10/31/2025) does not meet sterility requirements for ophthalmic use.
Thrive Health Solutions is recalling NAD+ 100mg/mL pre-filled syringes (Lot GA37484) because the manufacturer cannot assure the product is sterile. The product was distributed nationwide.
NatureMills US Incorporated is recalling Nature Mills Tomato Vadam (100g) because the product contains undeclared wheat allergen. Consumers with wheat allergies risk allergic reaction if they consume the product.
Terumo Cardiovascular Systems is recalling CDI OneView System BPM Probe units due to thermistor assembly errors that cause inaccurate temperature and blood gas measurements, potentially leading to inappropriate clinical decisions.
NatureMills US Incorporated is recalling Nature Mills Garlic Vadam (100g) distributed nationwide via its website because the product contains undeclared wheat allergens.
Becton Dickinson is recalling a specific lot of BD Insyte Autoguard BC Winged IV catheters (REF 382633, Lot 4222721) due to reports that the catheter needle may be slow to retract or fail to retract entirely.
NatureMills US Incorporated is recalling Nature Mills Black Kavuni Porridge Mix (200g) because it contains undeclared wheat allergens. Consumers with wheat allergies should not consume this product.
NatureMills US Incorporated is recalling Nature Mills Traditional Rasam Powder (200g) because it contains undeclared sesame and wheat allergens that are not listed on the label.
Encore Medical is recalling Altivate Reverse Torx Peripheral screws because the package labeling lists a different screw size than what is actually included in the package.
NatureMills US Incorporated is recalling NatureMills Avarampoo Soup (100g) because the product contains wheat that is not declared on the label, posing a risk to consumers with wheat allergies.
Bigfoot Biomedical is recalling Bigfoot Unity Diabetes Management System Pen Caps due to a firmware issue that may cause insulin pens to become unresponsive. People with diabetes may lack information needed to make timely treatment decisions.
Limacorporate S.p.A is recalling PRIMA 4MM Eccentrical Adaptor with Screw devices because the black laser marking used to identify positioning may be missing. The defect could affect proper device placement during use.
GE Healthcare is recalling the LOGIQ F R3 ultrasound system because it may display previous obstetric patient data in fetal weight measurements, potentially leading to incorrect clinical decisions about fetal size and growth.
Element 112, LLC is recalling Madeline's Patisserie Chocolate Croissants due to undeclared wheat. Consumers with wheat allergies could be at risk.
Becton Dickinson is recalling BD Insyte Autoguard Shielded IV Catheters (20 GA x 1.16 in, REF 381434) because the catheter needle may be slow to retract or fail to retract entirely.
NatureMills US Incorporated is recalling Idly Chili Powder 200g because it contains undeclared wheat, a common allergen that poses a risk to consumers with wheat allergies.
Becton Dickinson is recalling one lot of BD Insyte Autoguard Shielded IV Catheters (REF 381433, 20GA x 1.00 in) due to reports that the catheter needle may retract slowly or fail to retract completely.
Becton Dickinson is recalling BD Insyte Autoguard Winged Shielded IV Catheters (Lot# 4282308) because the catheter needle may be slow to retract or fail to retract entirely following use.
Becton Dickinson is recalling BD Insyte Autoguard BC Pro Winged Shielded IV Catheters (REF 382944) due to reports that the catheter needle may retract slowly or fail to retract completely.
NatureMills US Incorporated is recalling NatureMills Curry Leaf Rice Mix (200g) because it contains undeclared wheat, which poses a risk to consumers with wheat allergies.
NatureMills US Incorporated is recalling NatureMills Moringa Rice Mix (200g) because it contains undeclared wheat allergens. Consumers with wheat allergies should not consume the product.
Encore Medical is recalling Altivate Reverse Torx Peripheral Screws because package labeling indicates a different screw size than the product actually included. This mismatch could lead to incorrect surgical implantation.
Becton Dickinson is recalling a specific lot of BD Insyte Autoguard Shielded IV Catheters due to reports that the catheter needle may be slow to retract or fail to retract.
Becton Dickinson is recalling BD Insyte Autoguard Shielded IV Catheters (REF 381423, 22GA X 1.00 IN) due to the possibility that the catheter needle may be slow to retract or fail to retract entirely.
Philips Spectral CT systems with affected software may experience unintended motion of the gantry or table that could lead to contact with operators or patients. Additional software issues may also affect CT performance.
Certain 2021 and 2024 Polestar 2 vehicles may lose brake function while coasting downhill and using One Pedal Drive mode. Polestar will provide a free over-the-air software update to fix the control module defect.
Becton Dickinson is recalling BD Insyte Autoguard Winged IV Catheters (Ref. 381533, Lot 4282452) because the catheter needle may be slow to retract or fail to retract entirely.
CareFusion is recalling BD Pyxis automated dispensing cabinets and related devices due to a software configuration issue that can prevent user access to the medication dispensing application. This may delay patient care when Microsoft patches are installed during system upgrades.
NatureMills US Incorporated is recalling Nature Mills Wonderberry Leaf Soup because it contains undeclared wheat allergen. Consumers with wheat allergies who purchased this product should not consume it.
Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer C11137 due to calibration issues where curves switch from passed to failed status due to system errors, potentially causing erroneous test results.
Becton Dickinson is recalling BD Insyte Autoguard BC Pro Winged Shielded IV Catheters (18 GA x 1.16 in, Lot 4208538) due to reports that the catheter needle may be slow to retract or fail to retract completely.
GE Healthcare Versana Premier R3 and LOGIQ F R3 ultrasound systems can display previous obstetric patient data in fetal weight measurement reports, potentially leading to incorrect clinical decisions based on inaccurate fetal size and growth calculations.
NatureMills US Incorporated is recalling NatureMills Dal Garlic Rice Mix, 200g, because the product contains undeclared milk and wheat allergens that are not listed on the label.
NatureMills US Incorporated is recalling Nature Mills Vallarai Rice Mix (200g) because it contains undeclared wheat allergen. The product was distributed throughout the USA via the firm's website.
NatureMills US Incorporated is recalling Nature Mills Horsegram Rice Mix (200g) due to undeclared wheat allergens. The product was distributed via the firm's website throughout the USA.
NatureMills US Incorporated is recalling Nature Mills Horsegram Soup 100g packets because they contain undeclared wheat, a major allergen. The product was distributed nationally via the company's website.
Firehook of Virginia is recalling Firehook Artisan Baked Crackers Classic Sea Salt because some packages contain Everything Bagel Crackers, which include sesame that is not listed on the label.
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