Archive
700 recalls were announced in June 2026.
Of the 700 recalls this month scored against our rubric, 0% are Critical, 20% are Severe.
Which agencies issued them
Albertsons store-made Salmon with Lemon Capellini Pasta meal is being recalled because the contains statement does not declare salmon. Nine units are affected.
Albertsons store-made Smoked Salmon & Feta Pasta Salad is being recalled because the contains statement does not declare salmon. 34 units are affected.
Covidien Mon-a-Therm General Purpose Temperature Probes, REF 90044, are being recalled because the devices lack FDA clearance. 1,775 units are affected.
B. Braun CESK Riverside Health System kits are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering the product unusable.
B. Braun Lyndon B Johnson Hospital spinal epidural kits are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering it unusable.
Albertsons store-made Pop Dots Coco & Hazelnut, 6 count, is being recalled because the contains statement does not declare hazelnut. 25 units are affected.
HiRes Ultra 3D CI HiFocus Mid Scala cochlear implants are being recalled due to an incorrect shelf-life expiration date. 36 units are affected.
B. Braun CESK Shands Jacksonville kits are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering the product unusable.
Albertsons store-made Snacker Salad Tuna Pickle is being recalled because the contains statement does not declare tuna. Seven units are affected.
Xyvona levorphanol tartrate tablets, 3 mg, are being recalled following FDA's denial of marketing the product under the proprietary name Xyvona.
Covidien Mon-a-Therm Esophageal Stethoscopes with Temperature Sensor 400TM, REF 90042, are being recalled because the devices lack FDA clearance. 23,000 units are affected.
Albertsons store-made Salmon Kabob with Citrus Lemon Marinade is being recalled because the contains statement does not declare salmon.
Covidien Mon-a-Therm general purpose temperature probes in size 9 Fr, REF 90050, are being recalled because the devices lack FDA clearance. 128,900 units are affected.
Xyvona levorphanol tartrate tablets, 2 mg, are being recalled following FDA's denial of marketing the product under the proprietary name Xyvona.
Philips Medical Systems is recalling 27 Philips Azurion 3M15 units because a software issue can cause unusable dark images during imaging procedures.
Albertsons store-made Cajun Salmon & Spanish Rice meal is being recalled because the contains statement does not declare salmon. 86 units are affected.
Covidien Shiley Tracheostomy Tubes with inner cannula, REF 6FEN, are being recalled following a customer complaint about incorrect display box labeling. 1,002 units are affected.
B. Braun BlockJocks Trays are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering the product unusable. 210 units are affected.
Albertsons store-made Shrimp Kabob 16-20 count with Kung Pao Marinade is being recalled because the contains statement does not declare shrimp.
Albertsons store-made Yellow Caramel Pecan Cakes are being recalled because the contains statement does not declare pecan. 39 units in total are affected.
Albertsons store-made Cake Yellow Fudge Pecan half 8-inch is being recalled because the contains statement does not declare pecan.
Albertsons store-made Salmon Wasabi Grilled is being recalled because the contains statement does not declare salmon. Two units are affected.
B. Braun SESK UPMC Double Catheter Trays are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering it unusable.
Albertsons store-made Tempura Shrimp with Thai Sweet Chili Sauce is being recalled because the contains statement does not declare shrimp. 14 units are affected.
Albertsons store-made Southwest Shrimp Bowls are being recalled because the contains statement does not declare shrimp. 23 units in total are affected.
B. Braun CESK Northside Anesthesia Trays are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering it unusable.
Albertsons store-made Shrimp P&D Cajun Seasoned is being recalled because the contains statement does not declare shrimp. 18 units are affected.
Albertsons store-made Salmon Pesto with Asparagus is being recalled because the contains statement does not declare salmon. 149 units are affected.
Albertsons store-made Salmon Sweet Chili Kosher is being recalled because the contains statement does not declare salmon.
Ford is recalling 2024 Explorer vehicles with 2.3L engines and 10R60 transmissions because an unintentional powertrain control module reset may damage the park system, increasing the risk of vehicle rollaway.
Ford is recalling 2015-2018 Focus and 2013-2016 Fusion vehicles previously repaired incorrectly under prior recalls. The clutch may fracture, causing transmission damage and fluid leaks that increase fire risk.
Ford is recalling 2014 F-150 vehicles previously repaired under recall 24V444 because a signal loss can cause unexpected downshifting, increasing crash risk.
Natural Gas Fuel Systems is recalling Cummins CNG fuel systems because the tank support bracket may deform in a side impact, potentially causing the tank to detach and leak fuel.
Vermeer is recalling 2002-2026 BC1800XL brush chipper trailers because the hydraulic jack may extend unexpectedly, increasing the risk of loss of vehicle control and injury.
Ford is recalling 2012-2018 Focus vehicles previously repaired under recall 18V735 because a malfunctioning Canister Purge Valve may cause the engine to stall while driving, increasing crash risk.
Ford is recalling 2018-2024 Expedition vehicles because chrome plating on the center console may peel, creating sharp edges that could injure occupants.
Ford is recalling 2,349 vehicles because the instrument cluster may display blank, hiding critical safety information and increasing crash risk.
Ford is recalling 2019 Lincoln Nautilus vehicles previously repaired under recall 19V031 because the lane center assist system may fail to detect if the driver's hands are off the steering wheel for a prolonged period.
Ford is recalling 2018 F-150 vehicles previously repaired under recall 17V669 due to a software defect that may cause unintended gear selection and loss of gear indication.
Ford is recalling 2018-2020 F-150 vehicles previously repaired under recall 20V097 because daytime running lamps may fail to dim, reducing visibility for other drivers.
Ford is recalling 4,445 2017 F-150 vehicles because the instrument cluster may lose power in cold temperatures, hiding critical safety information like gear position.
Ford is recalling 2017 Escape vehicles previously repaired under recall 16V617 because power windows may exert excessive force before reversing, increasing injury risk.
Alliance RV is recalling certain Midwest Automotive Design recreational vehicles because the ground wire may be undersized for the electrical system, risking overheating and fire.
Yamaha is recalling 4,173 2025 XTZ690 motorcycles because the turn signal lights may fail to operate, increasing crash risk.
Little Grape Land Nursing Pillows are being recalled due to a risk of serious injury or death from suffocation. The pillows violate mandatory safety standards for nursing pillows and infant support cushions. No injuries have been reported.
Honda is recalling specific 2014-2023 vehicles because rear subframe corrosion can cause suspension failure, increasing crash risk.
Wyze Labs is recalling about 321,360 Solar Cam Pan security cameras because incorrect assembly instructions can cause the lithium-ion battery to overheat and catch fire. The firm has received 13 reports of overheating, six of fires, and six reports of minor burns.
SUNS International is recalling about 7,000 SS6291 Solenoid Interlock Switches used in residential elevators because they can become stuck, allowing the exterior door to remain unlocked and creating a risk of death or serious injury.
Chrysler is recalling 2020-2022 Pacifica Plug-In Hybrid Electric vehicles because the battery pack may cause a fire, even when parked.
International Motors is recalling 2027 IC Bus CESB school buses because wheelchair retractors may not lock, increasing injury risk.
Chrysler is recalling 2021-2025 Jeep Wrangler and Gladiator vehicles because steering pump wiring may overheat and cause a fire.
Vornado is recalling about 255,000 SRTH small room tower heaters because the fan blade can detach, causing overheating and fire. Vornado has received 32 overheating reports, including eight fires and one smoke inhalation.
Broqixin pool drain covers violate federal safety standards and pose a risk of serious injury or death from entrapment and drowning. About 370 units sold on Amazon from January to April 2026 should be removed immediately.
Crenlux pool drain covers violate federal safety standards and pose risks of entrapment and drowning. About 200 units sold on Amazon from June 2025 through March 2026 are affected.
TOMY International is recalling Boon NURSH 8 oz Reusable Baby Bottles because the hard plastic outer shell can bubble or peel, creating loose plastic pieces that pose a choking hazard to young children. No injuries have been reported.
Honda is recalling 2023-2026 CR-V Hybrid, Accord Hybrid, and 2025-2026 CR-V Fuel Cell EVs because the tire repair kit sealant bottle cap may detach and become a projectile.
Gudook Adult Bike Helmets (model KY-055, batch 202503, March 2025 manufacture) violate mandatory safety standards and fail to protect users in a crash, posing a serious risk of head injury or death. About 520 units sold on Amazon from May 2025 through February 2026.
Tiny Land Inc. is recalling about 7,500 children's play tents because fiberglass poles can shed fibers, causing skin and eye irritation. Consumers should stop using the tents immediately and contact Tiny Land for a free repair kit with plastic replacement poles.
Medline Industries, LP is recalling specific Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection due to microbiology testing data integrity concerns and efficacy complaints.
Medline Industries, LP is recalling Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection due to microbiology testing data integrity concerns and efficacy complaints.
Medline spinal block trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 30,120 kits are affected.
Medline spinal trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled over microbiology data integrity and efficacy complaints.
Medline spinal anesthesia trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 200,702 kits are affected.
Automated Impella Controllers sold outside the US are being recalled over alarm failures, power-path faults, electrical-short risks, inaccurate motor-current sensing and purge cassette misalignment.
Wawa Diet Lemonade in 16 oz plastic bottles is being recalled because of an undeclared milk allergen. 374 units are affected.
Aston Martin is recalling 2024 Valkyrie vehicles with track suspension because a deforming brake seal can cause overheating and fire risk.
Parmesan & Herb Bagel Crisps from Legacy Bakehouse are being recalled because they were made with recalled California Dairies milk powder over Salmonella.
Medline anesthesia trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 1,100 kits are affected.
Butter Parsley Bagel Crisps from Legacy Bakehouse are being recalled because they were made with recalled California Dairies milk powder over Salmonella.
Wawa Fruit Punch in 16 oz plastic bottles is being recalled because of an undeclared milk allergen. 1,694 units are affected.
Medline pain trays and Whitacre spinal block trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 28,106 kits are affected.
Giant Eagle Baked Pita Chips with Parmesan, Garlic & Herb Bagel Crisps are being recalled because they were made with recalled California Dairies milk powder over Salmonella.
Automated Impella Controllers that have not been through Abiomed's servicing process are pending four hardware updates addressing motor control, startup and pump stop risks.
The RelayPro Thoracic Stent-Graft System is subject to a labeling update concerning proximal clasp disconnection from the outer control tube, which may prevent release of the graft.
Wawa Diet Iced Tea Lemon in 16 oz plastic bottles is being recalled because of an undeclared milk allergen. 616 units are affected.
A bulk banana smoothie base is being recalled because the firm received and used a potentially Salmonella-contaminated ingredient to manufacture various products. 4,980 pounds are affected.
GE HealthCare ApexPro v6.0 eDelivery Software is being recalled because a persistent NO COMM or OFF NETWORK condition can cause potential loss of ECG and SpO2 monitoring.
GE HealthCare CARESCAPE Telemetry Servers ARK-2250L are being recalled because a persistent NO COMM or OFF NETWORK condition can cause potential loss of ECG and SpO2 monitoring.
Philips Azurion interventional X-ray systems are being recalled because hard drives in the system PCs may lose performance as they age, potentially causing loss of imaging functionality.
GE HealthCare is recalling CARESCAPE Telemetry Server V5 ATO models because a persistent NO COMM or OFF NETWORK condition can cause potential loss of ECG and SpO2 monitoring.
Fly By Jing Creamy Sesame Noodles are being recalled because possible cross-contamination resulted in an undeclared peanut allergen. 3,419 cases are affected.
Philips Allura Xper interventional X-ray systems are being recalled because hard drives in the system PCs may lose performance as they age, potentially causing loss of imaging functionality.
Halyard Purezero Ultraviolet Nitrile Exam Gloves are being recalled because they failed to meet specifications for chemical permeation performance. 452,500 units are affected.
Jayco is recalling 2026 Entegra and Jayco recreational vehicles because the taillight warning light may illuminate incorrectly, potentially confusing drivers and increasing crash risk.
Wawa Beverage Company is recalling Wawa Iced Tea Lemon 16 oz Pint plastic bottles because they contain undeclared milk.
HydroMARK Breast Biopsy Site Markers are being recalled because boxes labeled as T3 markers may contain individual packages labeled as T4 markers. 1,910 units are affected.
GE HealthCare IOU assemblies for the ARK2250 CARESCAPE Telemetry Server are being recalled because a persistent NO COMM or OFF NETWORK condition can cause loss of monitoring.
GE HealthCare ApexPro v5.0 Software Disaster Recovery USB Kits are being recalled because a persistent NO COMM or OFF NETWORK condition can cause loss of ECG and SpO2 monitoring.
GE HealthCare is recalling trade-in CARESCAPE Telemetry Servers because a persistent NO COMM or OFF NETWORK condition can cause potential loss of ECG and SpO2 monitoring.
Jayco is recalling 2026 Melbourne Prestige and Entegra Qwest recreational vehicles because the taillight warning light may illuminate incorrectly, potentially confusing drivers and increasing crash risk.
Medline EYE TRAY-LF kits are being recalled because they contain Cardinal Health syringes packaged as 1 mL tuberculin syringes but which are actually U-100 insulin syringes.
Medtronic 2x4 Pocket Adaptor Kits for Deep Brain Stimulation, model 64002, are being recalled because a limited number are labeled with incorrect use-by dates.
Medtronic 1x4 Pocket Adaptor Kits for Deep Brain Stimulation, model 64001, are being recalled because a limited number are labeled with incorrect use-by dates. 275 units are affected.
Nicotine Transdermal System Patches, 14 mg, distributed by Rugby Laboratories are being recalled after elevated oxidative-related impurities exceeded shelf-life specifications.
Pred Mild prednisolone acetate ophthalmic suspension 0.12% is being recalled after failing stability specifications. 2,736 bottles are affected.
Braun is recalling 2026 Ram ProMaster vehicles with specific wheelchair seat belts that may have incompatible connectors and fail to restrain occupants.
Kia is recalling 2027 Telluride and Telluride Hybrid vehicles because the driver seat belt may fail to extend, increasing injury risk in a crash.
Nova Bus is recalling LFS and LFS Artic transit buses because the low brake air pressure warning light may fail to illuminate when the engine is off, increasing crash risk.
Chrysler is recalling 2023-2026 Pacifica and Voyager vehicles because a spring may prevent air bags from deploying, increasing injury risk.
Grand Design is recalling 2025-2026 Reflection fifth wheel trailers because incorrectly tightened shock bolts may detach, creating a road hazard.
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