Recalls in November 2025 (page 2)
177 recalls.
- Ritz Peanut Butter Cracker Sandwiches recall (Mondelez Global Llc)
FoodClass IIReported December 31, 2025 · Undeclared allergens (Peanut) due to mispackaging - Zen Cleanse Blend herbal tea recall (Bell Industries LLC)
FoodClass IIReported December 31, 2025 · Potential Salmonella contamination - Restore Clinician Programmer Application recall (Medtronic Neuromodulation)
Medical deviceClass IIReported December 31, 2025 · Software issue where a Device Reset message displayed on the app was unable to be cleared. In rare cases, this resulted in an inability to resume therapy, and... - R¿sch-Uchida Transjugular Liver Access Sets recall (Cook Incorporated)
Medical deviceClass IIReported December 31, 2025 · Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut... - Ring Transjugular Intrahepatic Access Sets recall (Cook Incorporated)
Medical deviceClass IIReported December 31, 2025 · Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut... - Flexor Check-Flo Introducers and Sets recall (Cook Incorporated)
Medical deviceClass IIReported December 31, 2025 · Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut... - LifeShield Drug Library Management recall (ICU Medical, Inc.)
Medical deviceClass IIReported December 31, 2025 · Software issue only allows Concentration Limits to be defined to one digit of precision past the decimal point (0.1) instead of three digits (0.001). If the... - LifeShield Drug Library Management recall (ICU Medical, Inc.)
Medical deviceClass IIReported December 31, 2025 · For certain customers, the Change Summary review option ceases to operate as expected for any migrated library after the migration has been completed. Users... - BD Pyxis MedStation ES recall (CareFusion 303, Inc.)
Medical deviceClass IIReported December 31, 2025 · Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a... - Brand Name: Alcon Laboratories recall (Alcon Research LLC)
Medical deviceClass IReported December 31, 2025 · Ophthalmic procedure packs may have incomplete seals affecting sterility. - Draeger Vapor 3000. Unheated recall (Draeger, Inc.)
Medical deviceClass IReported December 31, 2025 · A certain component of affected devices was not delivered within specification and contained impurities. - Draeger Vapor 2000. Unheated recall (Draeger, Inc.)
Medical deviceClass IReported December 31, 2025 · A certain component of affected devices was not delivered within specification and contained impurities. - Brand name: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Common... recall (AGFA Healthcare Corp.)
Medical deviceClass IIReported December 31, 2025 · It is possible to exceed the maximum allowed Air Kerma rate (AKR) of 88mGy/min for pulsed fluoro exams. This can happen in case the framerate is increased on... - Celebration Herbals Senna Leaf Herbal Tea 24 Teabags recall (CELEBRATION HERBALS US)
FoodClass IIReported December 24, 2025 · possible salmonella - SENNA LEAVES F/C OG Item No: SEN15001 Net Wt: 44.75 Lbs Distributed By Whole Herb... recall (The Whole Herb Company, Inc.)
FoodClass IReported December 24, 2025 · Potential contamination with Salmonella. - Chef brand Milk Pan 24cm recall (Shata Traders Inc.)
FoodClass IIReported December 24, 2025 · Products found to contain leachable lead levels (3.00 mg/L) - Ondansetron ODT Tablets recall (Preferred Pharmaceuticals, Inc.)
DrugClass IIReported December 24, 2025 · Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets... - Cisatracurium Besylate Injection USP recall (SOMERSET THERAPEUTICS LLC)
DrugClass IIIReported December 24, 2025 · Subpotent product:out of specification assay results observed during long term stability testing. - Cisatracurium Besylate Injection USP recall (SOMERSET THERAPEUTICS LLC)
DrugClass IIIReported December 24, 2025 · Subpotent product:out of specification assay results observed during long term stability testing. - Cisatracurium Besylate Injection USP recall (SOMERSET THERAPEUTICS LLC)
DrugClass IIIReported December 24, 2025 · Subpotent product:out of specification assay results observed during long term stability testing. - Baclofen Tablets USP recall (Golden State Medical Supply Inc.)
DrugClass IIReported December 24, 2025 · Presence of Foreign Tablets/Capsules - BIOSURE HA SCREW recall (Smith & Nephew, Inc.)
Medical deviceClass IIReported December 24, 2025 · Removal of affected lot of screws due to labeling error. - Intelerad InteleShare software recall (DICOM Grid, Inc.)
Medical deviceClass IIReported December 24, 2025 · Software intended to aid in diagnosing conditions, planning treatments, visualizing anatomical structures has a bug that, if all of following are met: Viewing... - HemosIL SynthAFax. Partial Thromboplastin Time Tests. recall (Instrumentation Laboratory)
Medical deviceClass IIIReported December 24, 2025 · Recalled lots were manufactured with double the amount of preservative concentration. - Orthofix NorthStar OCT Navigation Surgical Technique Guide recall (SEASPINE ORTHOPEDICS CORPORATION)
Medical deviceClass IIReported December 24, 2025 · The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly identified both Medtronic s Solera and Medtronic s Infinity system toolcards as... - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported December 24, 2025 · Potential for incomplete seal on header bag. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported December 24, 2025 · Potential for incomplete seal on header bag. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported December 24, 2025 · Potential for incomplete seal on header bag. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported December 24, 2025 · Potential for incomplete seal on header bag. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported December 24, 2025 · Potential for incomplete seal on header bag. - Zimmer Dermatome AN recall (Zimmer Surgical Inc)
Medical deviceClass IIReported December 24, 2025 · The devices may have a misaligned thickness control bar. - Zimmer Air Dermatome recall (Zimmer Surgical Inc)
Medical deviceClass IIReported December 24, 2025 · The devices may have a misaligned thickness control bar. - Hardware configuration of the BeneVision Central Monitoring System recall (Mindray DS USA, Inc. dba Mindray North America)
Medical deviceClass IIReported December 24, 2025 · When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen freezing. - GE Healthcare Carestation anesthesia system Power Management Board recall (GE Medical Systems China Co., Ltd.)
Medical deviceClass IReported December 24, 2025 · Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is... - GE Healthcare Carestation anesthesia system recall (GE Medical Systems China Co., Ltd.)
Medical deviceClass IReported December 24, 2025 · Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is... - GE Healthcare Carestation anesthesia system recall (GE Medical Systems China Co., Ltd.)
Medical deviceClass IReported December 24, 2025 · Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is... - Ivenix Infusion System recall (Fresenius Kabi USA, LLC)
Medical deviceClass IReported December 24, 2025 · Software version 5.10.1 and earlier contain anomalies that have the potential to cause serious patient harm or death. - Prairie Farms Fat Free Milk recall (Prairie Farms Dairy)
FoodClass IIReported December 17, 2025 · Product may contain food-grade cleaning agents - Outer-packaging: gimme! brand Decaf de Agua coffee pods recall (Gimme Coffee, Inc.)
FoodClass IIReported December 17, 2025 · Undeclared caffeine - Charlevoix Cheese Company Mild Cheddar Cheese recall (Boss Dairy Farms)
FoodClass IReported December 17, 2025 · Possible Listeria monocytogenes contamination. - Simplot¿ Traditional Reduced Sodium Tater Gems¿ recall (JR Simplot Company)
FoodClass IIReported December 17, 2025 · Plastic fragments. Pieces of semi-rigid plastic embedded in the recalled Tater Gems product. - Doughy brand Chocolate Chip Cookie Dough recall (HUDSON RIVER FOODS CORP)
FoodClass IReported December 17, 2025 · Product may be contaminated with Salmonella - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported December 17, 2025 · CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits. - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported December 17, 2025 · CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits. - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported December 17, 2025 · CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits. - Morphine Sulfate Oral Solution 100 mg / 5 mL recall (Winder Laboratories, LLC)
DrugClass IIIReported December 17, 2025 · Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton. - Nebivolol Tablets recall (Glenmark Pharmaceuticals Inc., USA)
DrugClass IIIReported December 17, 2025 · Cross Contamination with Other Products - Tropicamide 1%/Cyclopentolate 1%/Phenylephrine 2.5%/Ketorolac 0.5% Topical Ophthalmic... recall (Fagron Compounding Services)
DrugClass IIReported December 17, 2025 · Incorrect Product Formulation - AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product... recall (Steris Corporation)
Medical deviceClass IIReported December 17, 2025 · Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within... - AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description:... recall (Steris Corporation)
Medical deviceClass IIReported December 17, 2025 · Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within... - Sonex brand aluminum pot recall (Alanwar Food Corp.)
FoodClass IReported December 10, 2025 · Products found to contain leachable lead levels (0.323mg/L) - Lava Bun with Salted Egg Yolk orange packaging recall (Prime Food Processing LLC.)
FoodClass IIReported December 10, 2025 · Products do not declare milk in the Contains statement or the ingredient statement. - Lava Bun with Green Tea Flavor bright lime green packaging recall (Prime Food Processing LLC.)
FoodClass IIReported December 10, 2025 · Products do not declare milk in the Contains statement or the ingredient statement. - Duloxetine Delayed-Release Capsules recall (Breckenridge Pharmaceutical, Inc.)
DrugClass IIReported December 10, 2025 · CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit - Duloxetine Delayed-Release Capsules recall (Breckenridge Pharmaceutical, Inc.)
DrugClass IIReported December 10, 2025 · CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit - Bisoprolol Fumarate and Hydrochlorothiazide Tablets recall (Glenmark Pharmaceuticals Inc., USA)
DrugClass IIIReported December 10, 2025 · Cross Contamination with Other Products: Testing of reserve samples showed presence of traces of ezetimibe - Face Rock Creamery Vampire Slayer Garlic Cheddar recall (FRC INC)
FoodClass IReported December 3, 2025 · FDA environmental sample identified the presence of Listeria monocytogenes in the processing area where cheese was packaged. - McLee Creations Recalls MyOnlyStyler Root Booster Hair Dryers Due to Risk of Serious Injury or Death from Electrocution and Shock Hazards
Consumer productReported November 26, 2025 · The handheld hair dryers lack an immersion protection device, which presents a substantial product hazard to consumers, posing the risk of death or serious... - Outdoor Master Children's and Youth Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold and Imported by Outdoor Master
Consumer productReported November 26, 2025 · The recalled children's and youth helmets violate the mandatory safety standard for bicycle helmets. Particularly, the helmets do not comply with the... - Convertible High Chairs Recalled Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards; Violate Mandatory Standard for High Chairs; Sold on Amazon by Rotinyard
Consumer productReported November 26, 2025 · The high chairs violate the mandatory standard for high chairs because they were sold without the required attached restraint system, posing a deadly fall... - Ozark Trail Tabletop 1-Burner Butane Camping Stoves Recalled Due to Serious Burn and Fire Hazards; Imported and Sold by Walmart; Manufactured by China Window Industry Co.
Consumer productReported November 26, 2025 · The stoves can explode or catch fire, posing a burn and fire hazard to consumers. - Sofoliana and Glotika Baby Loungers Recalled Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products; Sold on Amazon by Bosen US
Consumer productReported November 26, 2025 · The recalled baby loungers violate the mandatory safety standard for Infant Sleep Products. The sides are too low to contain an infant and the enclosed... - Vivohome Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation Hazards; Violates Mandatory Standard for Adult Portable Bed Rails; Imported by Vivohome
Consumer productReported November 26, 2025 · The recalled bed rails violate the mandatory standard for adult portable bed rails, posing a serious entrapment hazard and risk of death by asphyxiation. When... - Ikuso Safety Gates Recalled Due to Risk of Serious Injury or Death to Children from Entrapment; Violates Mandatory Standard for Gates and Enclosures; Sold on Amazon by Ikuso
Consumer productReported November 26, 2025 · The recalled gates violate the mandatory standard for expansion gates and expandable enclosures because a child's torso can fit through the opening between the... - Macardac Baby Loungers Recalled Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products; Sold on Amazon by Macardac Products
Consumer productReported November 26, 2025 · The recalled baby loungers violate the mandatory safety standard for Infant Sleep Products. The sides are too low to contain an infant and the enclosed... - Alinux Baby Loungers Recalled Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products; Sold on Amazon by Winkids
Consumer productReported November 26, 2025 · The recalled baby loungers violate the mandatory safety standard for Infant Sleep Products. The sides are too low to contain an infant and the enclosed... - KingPavonini Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by KingPavonini
Consumer productReported November 26, 2025 · The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped... - Ebern Designs Ojaswi 12-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violates Mandatory Standard for Clothing Storage Units; Manufactured and Sold by Ebern Designs
Consumer productReported November 26, 2025 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in serious injuries or death to... - Romorgniz Fabric 12- and 13-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violates Mandatory Standard for Clothing Storage Units; Sold on Amazon by Romorgniz
Consumer productReported November 20, 2025 · The recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazards that can result in injuries or death to... - Magnet Fidget Spinner Sets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Anzmtosn
Consumer productReported November 20, 2025 · The recalled magnet spinner sets violate the mandatory standard for toys because the sets contain loose magnets, posing an ingestion hazard to children. When... - Spartan Mowers and UTVs Recalls Riding Mowers Due to Crash Hazard
Consumer productReported November 20, 2025 · The riding mower's steering arm dampers can be installed incorrectly, which can result in an unexpected bouncing motion and loss of operator control, posing a... - Demlar Recalls MoonSoll and Magic Chems Fuel Bottles Due to Risk of Serious Injury or Death from Flash Fire; Violates Mandatory Standard for Portable Fuel Containers and FHSA Labeling Requirements; Imported by Demlar Online Store
Consumer productReported November 20, 2025 · The ethanol fuel bottles violate the federal safety standard for portable fuel containers because they lack flame mitigation devices required by the Portable... - Mallimoda Children's Pajama Sets Recalled Due to Risk of Serious Injury or Death from Burn Hazard; Violates Mandatory Standards for Children's Sleepwear; Sold on Amazon by Mallimoda
Consumer productReported November 20, 2025 · The recalled pajama sets violate the mandatory standards for children's sleepwear, posing a risk of serious injuries or deadly burn hazard to children. - Play Yards Recalled Due to Risk of Serious Injury or Death from Suffocation and Entrapment Hazards; Violate Mandatory Standard for Play Yards; Sold on Amazon by Anna Queen
Consumer productReported November 20, 2025 · The play yards violate the mandatory standard for play yards. Infants can become entrapped under the mattress or between the side of the play yard and the... - Little Partners Recalls Children's Grow 'N Stow Folding Learning Towers Due to Fall Hazard
Consumer productReported November 20, 2025 · The platform inside the tower can collapse, posing a fall hazard to young children. - Bearlala Baby Loungers Recalled Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products; Sold on Walmart.com by Nuoxuann
Consumer productReported November 20, 2025 · The recalled baby loungers violate the mandatory standard for Infant Sleep Products. The sides are too low to contain an infant. The enclosed openings at the... - AliExpress Recalls Convertible Strollers Due to Risk of Serious Injury or Death from Fall Hazard; Violates Mandatory Standard for Strollers
Consumer productReported November 20, 2025 · The stroller violates the mandatory standard for strollers because the restraint system can fail, posing a risk of serious injury or deadly fall hazard.