Archive
393 recalls were announced in January 2026.
Of the 393 recalls this month scored against our rubric, 10% are Critical, 8% are Severe.
Which agencies issued them
AVID Medical is recalling 380 Halyard Mini Plus Kit South units because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.
AVID Medical is recalling 52 Halyard Organ Recovery OR Packs because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.
Ambriola is recalling 179 bags of Ambriola Piccante grated Pecorino Romano in 5 and 10-pound sizes after the product tested positive for Listeria monocytogenes.
Ambriola is recalling 405 five-pound bags of Boar's Head Pecorino Romano Grated after the product tested positive for Listeria monocytogenes.
Securitas Healthcare is recalling 1,898 Arial 900 MHz Call Stations, model CSK200-900MR, because a firmware issue may prevent a low battery alert being transmitted before the battery fails.
CareFusion 303 is recalling 2,079 BD Pyxis ES Enterprise Server systems over a software issue that may result in equipment not receiving timely updates of patient or medication information.
Town Food Service Equipment is recalling approximately 11,300 aluminum sauce pans in 1QT to 3QT sizes after the product was found to contain leachable lead levels.
Fresh & Ready Foods is recalling 278 units of Fresh to You Spicy Veggie Breakfast Burrito over foreign material.
Meijer is recalling 38,043 gallons of Meijer Steam Distilled Water because of a floating black foreign substance in the product.
Remote Diagnostic Technologies is recalling 7,129 Philips Tempus Pro Patient Monitors because intracranial and bladder pressure measurements have not been tested or validated for accuracy.
Medline is recalling 1,611,081 Hudson RCI medium concentration oxygen masks after multiple complaints of tubing disconnecting, which may lead to shortness of breath and hypoxia.
Direct Source Seafood is recalling 3,290 cases of Market 32 by Price Chopper frozen raw shrimp because the shrimp may be contaminated with Cesium-137.
Imprimis NJOF is recalling 596 boxes containing 11,920 pre-filled syringes of Dexamethasone, Moxifloxacin and Ketorolac intraocular injection over glass-like particles.
Imprimis NJOF is recalling 314 boxes containing 6,280 pre-filled syringes of Tri-Moxi triamcinolone and moxifloxacin intraocular injection over glass-like particles.
Imprimis NJOF is recalling 778 boxes containing 15,540 pre-filled syringes of Dexamethasone and Moxifloxacin intraocular injection over glass-like particles.
Securitas Healthcare is recalling 5,627 Arial 900 MHz Call Stations, model CSK200-900, because a firmware issue may prevent a low battery alert being transmitted before the battery fails.
Direct Source Seafood is recalling 1,800 cases of waterfront BISTRO frozen raw shrimp, sold alongside Market 32 brand shrimp, because the shrimp may be contaminated with Cesium-137.
Roche Diagnostics is recalling 1,300 Elecsys Anti-TSHR cassettes because results vary by instrument platform and calibrator lots vary, which may lead to incorrect diagnosis or treatment.
Fresh & Ready Foods is recalling 93 units of Sprig & Sprout Spicy Breakfast Burrito over foreign material.
D. Coluccio & Sons is recalling 800 units of Sapori Amaretti Almonds cookies because the product contains elevated levels of hydrocyanic acid.
Meridian Bioscience is recalling 211 units of the Revogene C. difficile assay because affected lots show a decline in performance over time, which may lead to false-negative results.
McCain Foods USA is recalling 21,256 cases of Ore-Ida Tater Tots shaped potatoes over clear hard plastic fragments.
Philips North America is recalling 13,470 Smart-hopping 2.0 AP 1.4 GHz patient monitors because the MX40 could not reconnect to the PIC iX when signal strength changed quickly.
Fresh & Ready Foods is recalling 62 units of Fresh to You Spicy Egg Potatoes Cheese Tacos over foreign material.
Fresh & Ready Foods is recalling 200 units of Evergreen Refreshments Eggs Potatoes Cheese Tacos over foreign material.
IMRIS Imaging is recalling 122 HFD100 Head Fixation Devices because a torque screw may crack or separate, which could lead to inadequate head stabilization and risk of patient injury.
MAYEJ Comercializadora is recalling 1,288 boxes of Italian Parsley over the pathogen Cyclospora cayetanensis.
McCain Foods USA is recalling 17,597 cases of Sysco Imperial Potato Tater Barrel over clear hard plastic fragments.
Philips Healthcare (Suzhou) is recalling 35 Incisive CT systems over the potential for an incomplete scan due to an unstable connection inside the floating sensor.
AvKARE is recalling 7,991 cartons of Rosuvastatin Tablets, USP 10 mg, because the product was out of specification for dissolution.
Integra LifeSciences is recalling 5,116 Codman CereLink ICP Sensor Basic Kits over potential corrosion stains on the surface of the 14-gauge Tuohy needle included in the kits.
Alembic Pharmaceuticals is recalling Fesoterodine Fumarate Extended-release Tablets, 8 mg, because levels of a diester impurity exceeded the specification limit.
Beckman Coulter is recalling 6,457 UniCel DxI 800 analyzers because a potential communication issue may prevent the instrument restarting after a standard shutdown, causing delayed results.
Ziyad Brothers Importing is recalling 2,865 cases of Baraka French Style Puff Pastry because the product may contain partially hydrogenated oils.
Rovira Biscuit is recalling 9,838 units of Tempting Crackers over undeclared colours FD&C Yellow #6 and FD&C Red 40.
Abiomed is recalling 6 Impella 5.5 with SmartAssist S2 sets because the device was packaged in an incorrect outer box carton.
Rovira Biscuit is recalling 71,492 units of Vanilla Treats Crackers and Mini Vanilla Treats over undeclared colours FD&C Yellow #6 and FD&C Red 40.
SpecGx is recalling 74,544 bottles of Oxycodone and Acetaminophen CII Tablets, 7.5 mg/325 mg, because of the potential for the imprint to be missing on tablets.
Rovira Biscuit is recalling 6,671 units of 100to en boca snack crackers over undeclared colours FD&C Yellow #6 and FD&C Red 40.
Rovira Biscuit is recalling 29,246 units of Tita Crackers over undeclared colours FD&C Yellow #6 and FD&C Red 40.
Siemens Medical Solutions is recalling LUMINOS Lotus Max and Luminos dRF Max systems because switching quickly between organ programs may result in incorrect collimation.
Beckman Coulter is recalling 1,272 UniCel DxI 600 analyzers because a potential communication issue may prevent the instrument restarting after a standard shutdown, causing delayed results.
Rovira Biscuit is recalling 22,114 units of Vanilla Econo, Galletas de Vainilla, over undeclared colours FD&C Yellow #6 and FD&C Red 40.
Signature Formulations is recalling 1,458 containers of ORL Kids Natural Toothpaste, bubblegum flavour, over current good manufacturing practice deviations.
Sophysa is recalling 105 Pressio 2 ICP Monitoring Systems following customer complaints of the Pressio monitor rebooting.
Rovira Biscuit is recalling 16,478 units of Great Value Vainilla Crackers over undeclared colours FD&C Yellow #6 and FD&C Red 40.
Applied Medical Resources is recalling 450 units of the Kii Low Profile Bladed Dual Pack because of the potential for extended length of the blade obturator after assembly.
Signature Formulations is recalling 570 bottles of ORL Kids Mouthwash, bubblegum flavour, over current good manufacturing practice deviations.
Integra LifeSciences is recalling 1,301 Codman Microsensor Basic Kits over potential corrosion stains on the surface of the 14-gauge Tuohy needle included in the kits.
Ziyad Brothers Importing is recalling 575 cases of Baraka Gourmet Pastry Kunafe because the product may contain partially hydrogenated oils.
SpecGx is recalling 287,988 bottles of Oxycodone and Acetaminophen CII Tablets, 10 mg/325 mg, because of the potential for the imprint to be missing on tablets.
Vision RT is recalling 56 AlignRT InBore systems because information identifying the lasers and their characteristics was omitted from the Instructions for Use.
East Trailers is recalling 2024-2026 Beast and Beast II trailers because an improper weld may cause the rear impact guard to detach, increasing crash injury risk.
Lippert is recalling 3000 Series Hidden Hinge Ramp Doors because they may break away from the frame during use, increasing the risk of injury.
Terex is recalling 2025 TL, LT, LTM40, HR40, HR46, and SCM55 aerial devices because a control valve defect may cause hydraulic equipment to overheat, posing a burn risk.
Jaguar Land Rover is recalling 2026 Range Rover Sport vehicles because the certification label lists incorrect weight information, which could lead to overloading.
Goodyear is recalling specific Cooper Discoverer SRX tires because incorrect Tire Identification Numbers prevent proper registration and compliance with federal safety standards.
About 3,500 Lterfear Multifunction Pounding Games are being recalled because they contain high-powered magnets that can detach, posing an ingestion hazard to children.
About 18,700 Julie and Judah pajama and lounge pants and shorts are being recalled because they violate the mandatory flammability standards for children's sleepwear.
About 55 SARO Braided Crib Bumpers, Model 1374, are being recalled because they can obstruct an infant's breathing and are banned under the Safe Sleep for Babies Act.
About 26,200 Sangohe adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and the mattress.
About 1,430 NFSVLB baby bath seats are being recalled because they are unstable, can tip over, and have leg openings that allow a child's torso to become entrapped.
About 13,200 Isla Rae magnetic wireless chargers are being recalled because the chargers can explode while in use, posing fire and burn hazards.
About 1,200 PNW Components Loam Pedal Gen 2 mountain bike pedals are being recalled because the pedal axle can crack, causing the pedal to detach from the crank.
About 320 RH 48-inch and 60-inch Natural Antler Chandeliers are being recalled because canopy hardware can break when hung at an angle, causing the fixture to fall.
About 9,300 Joyful Journeys baby loungers are being recalled because the sides are too low, the foot openings are too wide, and the loungers have no stand.
About 870 Rattan 6-Drawer Dressers, model YD001, are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
About 5,000 Agrish adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and the mattress.
About 14,250 YOLAAH bed rails, model BR-01, are being recalled because users can become entrapped within the rail or between the rail and the mattress.
About 60,250 DR Power walk-behind and tow-behind leaf vacuums are being recalled because pieces can come loose inside the unit or debris can pierce the chute, ejecting material.
About 2,240 Kori Gey water elf toy kits are being recalled because the button cell battery compartment can be easily accessed and opened by children.
About 4,155 Vasicar 18-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
About 280 BabyBond retractable safety gates are being recalled because a child's torso can fit through the opening between the gate and the floor and become entrapped.
Wanli Tire Corporation is recalling Aptany Eco Sendero M/T2 tires because the sidewall may separate, increasing the risk of a crash.
Tom Bumble is recalling approximately 6,500 units of Nutty Peanut Butter Flake Candy with Peanut & Chocolate over foreign material.
Novo Nordisk is recalling Wegovy (semaglutide) Injection, 0.5 mg/0.5 mL prefilled pens, over the presence of particulate matter after hair was found in a prefilled syringe.
Shenzhen Atomstack Technologies is recalling material processing laser products for lacking a remote interlock connector required under 21 CFR 1040.10(f)(3).
Novo Nordisk is recalling Wegovy (semaglutide) Injection, 1 mg/0.5 mL prefilled pens, over the presence of particulate matter after hair was found in a prefilled syringe.
Sheathing Technologies is recalling 12 units of Sheathes3D vaginal and rectal ultrasound probe covers because product defects may result in contamination during use, posing an infection risk.
Indian Cookware and Appliance is recalling 10 pieces of Aluminium Hammered Kadai Size 7 over potential contamination due to leachable lead.
CareFusion 213 is recalling 106,400 units of BD ChloraPrep Triple Swabsticks over a lack of assurance of sterility.
Glenmark Pharmaceuticals is recalling 96,948 packs of Ondansetron Orally Disintegrating Tablets, 4mg, because the blister packs are not fully sealed and tablets are falling out.
Beaver-Visitec International is recalling 5 BVI Leos Laser and Endoscopy Systems because ferrites specified for the USB cable assembly were not installed as intended.
Philips Ultrasound is recalling 1,721 EPIQ Ultrasound Systems used with the X5-1c transducer because the system may experience an unexpected automatic reboot, resulting in damage to the transducer.
Ferndale Laboratories is recalling 24,589 units of Mastisol Liquid Adhesive because the butyrate tube cracks during actuation, rendering the product unusable.
Vortex Surgical is recalling 221 units of its 25ga Illuminated Flex-Tip Laser Probe because some products in the lot are not passing through a 25ga cannula smoothly.
Bendon Publishing is recalling 39,171 units of Paw Patrol and Mickey Mouse heart-shaped gummy candies over an unapproved color additive, chlorophyllin copper complex.
Zydus Pharmaceuticals is recalling 2,136 bottles of traZODONE Hydrochloride Tablets, 100mg, after a product complaint that some tablets had a dent on the plain side of the tablet surface.
Blue Bird is recalling 2026 Vision and All American electric transit buses because wheelchair restraints may fail to lock, increasing injury risk.
Rivian is recalling certain 2022-2025 R1S and R1T vehicles that previously had service performed, because the toe link may have been reassembled incorrectly and the joint may separate.
Blue Bird is recalling 2022-2024 All American electric transit buses because a loose 12-volt cable may disconnect, causing loss of electrical systems and increasing crash risk.
Allwin Powersports is recalling specific LS2 Rebellion helmets that may lack proper impact protection, increasing the risk of injury during a crash.
Volvo Car USA is recalling 40 model year 2025 EX30 vehicles because the high-voltage battery may experience a short circuit and overheat, increasing fire risk.
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