Archive
554 recalls were announced in February 2026.
Of the 554 recalls this month scored against our rubric, 9% are Critical, 11% are Severe.
Which agencies issued them
Philips is recalling 802 units of the Azurion 3 M15 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
McCain Foods USA is recalling 67 cases of Sonic Tots frozen potato product over foreign material described as small hard plastic fragments.
Medline is recalling 7,570 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Medline is recalling 1,350 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Ventura Foods is recalling 17 after the firm found pieces of blue plastic in a filter during production.
Cacao Art is recalling 128 Crunchy Caramel artisan dark chocolate bars because the product contains butter but milk is not declared in the ingredients or a contains statement.
Elekta is recalling Leksell GammaPlan version 11.1 because an error when defining a new stereotactic reference may produce a treatment plan that irradiates the incorrect patient location.
Elekta is recalling Leksell GammaPlan versions 11.3 and 11.4 because an error when defining a new stereotactic reference may produce a treatment plan that irradiates the incorrect patient location.
Asteria Health is recalling 670 pellets of Testosterone 75mg, Anastrozole 4mg sterile pellets over the potential presence of metal particulate matter.
Philips is recalling 3 units of the Spectral CT 7500 on Rails because fasteners attaching the rotor to the gantry bearing may not be torqued to specification.
Philips is recalling 283 Spectral CT units because fasteners attaching the rotor to the gantry bearing may not be torqued to specification.
Philips is recalling 291 units of the Azurion 3 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Asteria Health is recalling 14,848 pellets of ESTRADIOL, 15 mg sterile pellets over the potential presence of metal particulate matter.
Karison Foods & Snacks is recalling 230 cases of Karison brand Besan Laddoo, 12 oz, because the product contains milk which is undeclared in the ingredient statement.
Philips is recalling 1 of the Azurion 7 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
McCain Foods USA is recalling 21,557 cases of Ore-Ida Tater Tots shaped potatoes over foreign material described as small hard plastic fragments.
TKS Co-pack Manufacturing is recalling 3,630 bottles of Aonic Complete Hers liquid dietary supplement over possible coliforms, E. coli and Pseudomonas aeruginosa contamination.
Philips is recalling 326 units of the Azurion 5 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Medline is recalling 8,445 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Asteria Health is recalling 2,442 pellets of ESTRADIOL, 25 mg sterile pellets over the potential presence of metal particulate matter.
Hologic is recalling 681,870 Brevera Breast Biopsy System disposable 9 gauge needles because particulates in affected devices can be deposited into breast tissue during use.
Asteria Health is recalling 194,336 pellets of Testosterone, 200 mg sterile pellets over the potential presence of metal particulate matter.
Philips is recalling 922 units of the Azurion 5 M20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Fresenius Kabi Compounding is recalling 1,410 bags of Ketamine HCl injection over a lack of assurance of sterility.
Medline is recalling 450 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Asteria Health is recalling 89,074 pellets of Testosterone, 25.0 mg sterile pellets over the potential presence of metal particulate matter.
Fresenius Kabi Compounding is recalling 1,578 bags of Vancomycin HCl injection over a lack of assurance of sterility.
Lee's Commissary is recalling 6,480 packages of Red Button Movie House Popcorn, 24 oz, because the product may contain foreign material.
Medline is recalling 4,300 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Karison Foods & Snacks is recalling 230 cases of Karison brand Alsi Pinni, 12 oz, because the product contains milk which is undeclared in the ingredient statement.
Asteria Health is recalling 153,498 pellets of Testosterone, 100 mg sterile pellets over the potential presence of metal particulate matter.
Medline is recalling 21,854 units of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Unichem Pharmaceuticals USA is recalling 60,000 Doxazosin Tablets, USP 4 mg, because the tablets are imprinted with the wrong ID.
Laerdal Medical is recalling 1,202 Compact Suction Unit 4 RTCA units because those made in a limited period may emit electromagnetic noise beyond the acceptable RTCA limits.
KPCM New York is recalling 720 bottles of Preema brand food colour powders because they contain the banned colour carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40.
Steris is recalling 10 units of the Barco MNA with HexaVue IP Integration System because the supplier used the incorrect configuration file for a limited batch of adapter components.
Domino Foods is recalling 2,023 cases of Sodexo Stars Saccharin (Pink) Packets over undeclared aspartame.
Pro Numb Tattoo Numbing Spray LLC is recalling Pro Numb Tattoo Numbing Spray For Sensitive Skin, 4% Lidocaine, over cGMP deviations.
Alphatec Spine is recalling 7 ATEC Lateral Navigation Disc Prep Instruments due to a design issue where the navigated array connection geometry is incorrect.
Meitheal Pharmaceuticals is recalling 16,477 Cetrorelix Acetate for Injection kits over a defective delivery system, with needles either missing from or duplicated within the kit.
Alphatec Spine is recalling 15 ATEC Lateral Navigation Disc Prep Instruments due to a design issue where the navigated array connection geometry is incorrect.
Pro Numb Tattoo Numbing Spray LLC is recalling Pro Numb Tattoo Numbing Spray, 5% Lidocaine, over cGMP deviations.
SurePulse Medical is recalling the Surepulse VS Cap Small because the labeling contains an incorrect sizing guide for the cap.
Straumann USA is recalling 561 WB Impression Post Closed Tray units because the impression caps provided in the package are magenta instead of brown.
SurePulse Medical is recalling the Surepulse VS Cap Extra Small because the labeling contains an incorrect sizing guide for the cap.
SurePulse Medical is recalling the Surepulse VS Cap Large because the labeling contains an incorrect sizing guide for the cap.
SurePulse Medical is recalling the Surepulse VS Cap Extra Large because the labeling contains an incorrect sizing guide for the cap.
SurePulse Medical is recalling the Surepulse VS Cap Medium because the labeling contains an incorrect sizing guide for the cap.
Prevost is recalling 2025-2026 X3-45 commuter buses because improperly installed seat anchors may not restrain occupants during a crash.
Winnebago is recalling certain 2020-2023 View and Navion recreational vehicles because the rear roof cap aerofence trim may become loose and detach during transit.
Ford is recalling 2025 Transit vehicles because the brake pedal may disconnect from the booster pushrod, causing a loss of brake function and increasing crash risk.
Ford is recalling certain 2022-2026 Escape and 2023-2026 Lincoln Corsair plug-in hybrids because a defect in one or more high voltage battery cells may cause an internal short circuit and battery failure.
Shyft Group is recalling 2024-2025 Blue Arc BA4L-800 vehicles because steering gearbox mounting fasteners may loosen, causing the gearbox to bind and increasing crash risk.
Couture Co Ltd is recalling Hyperax Volt RV 4x bike carriers because vibrations may cause anchoring plates to fail, allowing the carrier or bike to detach from the vehicle.
GM is recalling certain 2022 Tahoe, Suburban, Yukon, Yukon XL, Escalade and Escalade ESV vehicles with the 10-speed ETRS transmission because the transmission control valve may fail and lock up the rear wheels.
Daimler Trucks North America is recalling 2,843 Thomas Built Buses Saf-T-Liner EFX and HDX school buses because improperly tightened heater hose clamps may cause hot coolant to leak inside the passenger compartment.
Daimler Trucks North America is recalling 2023-2026 Thomas Built Buses Saf-T-Liner EFX and HDX models because improperly tightened heater hose clamps may cause hot coolant to leak into the passenger compartment.
GM is recalling certain Chevrolet Silverado and GMC Sierra vehicles that may have been repaired incorrectly under recall 24V797, because the transmission control valve may fail and lock the rear wheels.
About 550 Fortemotus-branded adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and the mattress.
About 166 SOOWERY 6-Drawer Dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children.
About 11,000 3-Pack Smoke Detector Fire Alarms are being recalled because if the sensing threshold is set too high, the alarm might not sound in a timely manner.
About 590 CheerKid baby bath seats are being recalled because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.
GM is recalling certain 2024 Cadillac Lyriq vehicles because the rearview camera screen may turn gray with no camera image.
About 800 Beloems-branded adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and the mattress.
About 1,200 Colombia-themed magnetic board games are being recalled because the magnetic game pieces contain loose high-powered magnets, posing an ingestion hazard to children.
About 32,900 hydromassage rotary jets in Highlife Collection spas are being recalled because the suction force can entangle a user's hair and submerge their head underwater.
International is recalling certain 2026-2027 MV vehicles because the ECU software may fail to engage the brakes when adaptive cruise control or hill hold assist is in use.
JUICE from the Raw, spicy lemonade is being recalled by Everpress Juice because the under-processed product may contain pathogenic bacteria that could harm humans.
JUICE from the Raw, cashew milk is being recalled by Everpress Juice because the under-processed product may contain pathogenic bacteria that could harm humans.
JUICE from the Raw, cashew coffee milk is being recalled by Everpress Juice because the under-processed product may contain pathogenic bacteria that could harm humans.
B.C. Williams Bakery Service is recalling 720 bags of Bread and Roll Mix, sold in 50 lb bags, over an undeclared milk allergen.
JUICE from the Raw, sweet greens is being recalled by Everpress Juice because the under-processed product may contain pathogenic bacteria that could harm humans.
JUICE from the Raw, pineapple mint is being recalled by Everpress Juice because the under-processed product may contain pathogenic bacteria that could harm humans.
Boston Scientific is recalling 150 HOT AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 8mm x 8mm, after increased reports of stent deployment and expansion issues.
Boston Scientific is recalling 557 AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 20mm x 10mm, after increased reports of stent deployment and expansion issues.
Green Lumber Holdings is recalling Green Lumber Natural Fuel For Men capsules because FDA analysis found the product to contain tadalafil, and it is marketed without an approved application.
Handelnine Global is recalling four bottles of Rheumacare capsules after the product was found to contain lead.
B.C. Williams Bakery Service is recalling 51 bags of Spice Cake Mix, sold in 50 lb bags, over an undeclared milk allergen.
Boston Scientific is recalling 39 AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 6mm x 8mm, after increased reports of stent deployment and expansion issues.
Tai Phat Wholesalers is recalling 10 cases of Sofit Seedless Red Dates, 12 oz, over undeclared sulfites.
JUICE from the Raw, upbeat is being recalled by Everpress Juice because the under-processed product may contain pathogenic bacteria that could harm humans.
Boston Scientific is recalling 588 units of the HOT AXIOS Stent and Electrocautery-Enhanced Delivery System, 20mm x 10mm after increased reports of stent deployment and expansion issues.
Boston Scientific is recalling 266 HOT AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 6mm x 8mm, after increased reports of stent deployment and expansion issues.
Boston Scientific is recalling 59 units of the AXIOS Stent and Electrocautery-Enhanced Delivery System, 8mm x 8mm after increased reports of stent deployment and expansion issues.
B.C. Williams Bakery Service is recalling 95 bags of Swiss Chocolate Cake Mix, sold in 50 lb bags, over an undeclared milk allergen.
VH Foods is recalling 4,497 packages of Outside The Breadbox brand Bread Crumbs, 8 oz, over undeclared egg and milk.
Tradin Organics USA is recalling 54,680 lbs of Organic Chia Seed Black over potential contamination with Salmonella.
JUICE from the Raw, Detox Greens is being recalled by Everpress Juice because the under-processed product may contain pathogenic bacteria that could harm humans.
Nissan is recalling certain 2023-2025 Rogue vehicles with the 1.5L VC-Turbo engine because increased temperatures can break down the engine oil, causing the bearings to seize and the engine to fail.
CS Beef Packers is recalling approximately 22,912 pounds of raw ground beef products that may be contaminated with E. coli O145. The products were distributed to foodservice locations in California, Idaho, and Oregon.
Nissan is recalling certain 2024-2025 Rogue vehicles with the 1.5L VC-Turbo engine because the gears in the electronic throttle body assembly may break, causing a loss of drive power.
General Rubber is recalling specific Xcellent Roadbreaker A/T tires that may crack and separate, increasing the risk of a crash.
Vortex Surgical is recalling 14,789 units because there may be voids in the seal of the Tyvek pouches, which compromises the sterile barrier.
Changchun Wancheng Bio-Electron is recalling 4,800 units of the Exploro Highly Sensitive Male Fertility / Sperm Concentration Test because tests requiring a 510(k) were distributed before they could be legally marketed.
Changchun Wancheng Bio-Electron is recalling 1,000 units of the LH One Step Ovulation Test Device (Urine) because tests requiring a 510(k) were distributed before they could be legally marketed.
Vortex Surgical is recalling 14,789 units because there may be voids in the seal of the Tyvek pouches, which compromises the sterile barrier.
Changchun Wancheng Bio-Electron is recalling 3,000 units of Vivoo Vaginal pH Test because tests requiring a 510(k) were distributed before they could be legally marketed.
Imu-Tek Animal Health is recalling 113 bottles of Imu-Tek Immuno-5 Colostrum Powder, 7 oz, over an undeclared milk allergen.
Diva Fam is recalling Sea Moss Gel Superfood in the Mango variety over potential Clostridium botulinum contamination.
Intuitive Surgical is recalling 219 da Vinci X, Xi and da Vinci 5 systems because a software error allowed instrument arms failing an important diagnostic test to remain in clinical use.
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