Recalls in March 2026 (page 3)
465 recalls.
- Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft -Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Olympus Thunderbeat II Shears w/Ultrasonic Mode recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for detachment of a distal tip component of the device during use. - Olympus Thunderbeat II Shears w/Ultrasonic Mode recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for detachment of a distal tip component of the device during use. - Olympus Thunderbeat II Shears w/Ultrasonic Mode recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for detachment of a distal tip component of the device during use. - Olympus Thunderbeat II Shears w/Ultrasonic Mode recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for detachment of a distal tip component of the device during use. - CUSA Clarity C7000 Console recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported April 29, 2026 · Software issue that renders the touch screen unresponsive. - The product is a handheld ultraviolet-C germicidal wand and contains a combination of... recall (Uvlizer c/o RAIS INTERNATIONAL LLC)
Medical deviceClass IIReported April 29, 2026 · In some foreseeable use conditions, the products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international... - The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure... recall (Uvlizer c/o RAIS INTERNATIONAL LLC)
Medical deviceClass IIReported April 29, 2026 · In some foreseeable use conditions, the Products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international... - Booey's Dragon's Breath sauce recall (Booey's Gourmet LLC)
FoodClass IIReported April 22, 2026 · Ingredients statement declares Anchovy and Sasame, but Contains statement does not declare Fish (Anchovy) and Sesame. - Raw & Unfiltered Bee Well Wildflower Honey recall (Bee Well Honey Farm & Supply Inc.)
FoodClass IIIReported April 22, 2026 · High sugar content. The firm was notified by the FDA that sample results were positive for a high C4 sugar content. - Magnesium Chloride recall (Avantor Performance Materials LLC)
DrugClass IIIReported April 22, 2026 · Subpotent drug - Memantine Hydrochloride Extended-Release recall (The Harvard Drug Group LLC)
DrugClass IIReported April 22, 2026 · Failed Dissolution Specifications - Essential Calming Skin Gel recall (Island Kinetics, Inc. d.b.a. CoValence Laboratories)
DrugClass IIIReported April 22, 2026 · Subpotent Drug - Skin Rehab recall (Island Kinetics, Inc. d.b.a. CoValence Laboratories)
DrugClass IIIReported April 22, 2026 · Subpotent Drug - Remedy Gel recall (Island Kinetics, Inc. d.b.a. CoValence Laboratories)
DrugClass IIIReported April 22, 2026 · Subpotent Drug - Albuterol Sulfate Inhalation Solution recall (Nephron SC, LLC)
DrugClass IIReported April 22, 2026 · Labelling: Illegible label - Fluocinonide recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIReported April 22, 2026 · Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing. - Fluocinonide recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIReported April 22, 2026 · Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing. - Fluocinonide recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIReported April 22, 2026 · Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing. - Semaglutide-Glycine-Cyanocobalamin Injectable recall (PAYLESS COMPOUNDERS, LLC)
DrugClass IIReported April 22, 2026 · Lack of Assurance of Sterility - QC Quality Choice recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - QC Quality Choice recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - QC Quality Choice recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - QC Quality Choice recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - QC Quality Choice recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - QC Quality Choice recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - QC Quality Choice recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - MGC Health recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - MGC Health recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - MGC Health recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - Discount Drug Mart Food Market recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - Discount Drug Mart Food Market recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - caring mill recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - exchange select recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - exchange select recall (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.)
DrugClass IIReported April 22, 2026 · This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing... - SLMD Benzoyl Peroxide Acne Lotion recall (Owen Biosciences Inc.)
DrugClass IIReported April 22, 2026 · Chemical contamination: Presence of benzene - SLMD BP Acne Spot Treatment recall (Owen Biosciences Inc.)
DrugClass IIReported April 22, 2026 · Chemical contamination: Presence of benzene - HydroPeptide CLEAR ALLIANCE SERUM recall (Owen Biosciences Inc.)
DrugClass IIReported April 22, 2026 · Chemical contamination: Presence of benzene - FHF Farmhouse Fresh recall (Owen Biosciences Inc.)
DrugClass IIReported April 22, 2026 · Chemical contamination: Presence of benzene - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported April 22, 2026 · CGMP Deviations; presence N-Nitroso Cinacalcet above the acceptable daily intake limit - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported April 22, 2026 · CGMP Deviations; presence N-Nitroso Cinacalcet above the acceptable daily intake limit - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported April 22, 2026 · CGMP Deviations; presence N-Nitroso Cinacalcet above the acceptable daily intake limit - Philips Spectral CT on Rails. Model Number: 728334. recall (PHILIPS MEDICAL SYSTEMS)
Medical deviceClass IIReported April 22, 2026 · Philips has identified three software issues: 1. During a continuous CT (CCT) scan, there is the potential that the Gantry could remain at the current scan... - CENTURION Circumcision Kit recall (Medline Industries, LP)
Medical deviceClass IIReported April 22, 2026 · On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile. - Gentuity HF-OCT Imaging System Model G10-01 recall (Gentuity, LLC)
Medical deviceClass IIReported April 22, 2026 · The potential for repeated frames during HF-OCT pullback when using the Gentuity HF-OCT Console (software version 21.11 to 23.3.13) with the Vis-Rx and Vis-Rx... - Cytal Burn Matrix 10x15 cm. Product ID: BMM1015. recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported April 22, 2026 · Increased rate of out-of-specification endotoxin results. - Cytal Burn Matrix 7x10 cm. Product ID: BMM0710. recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported April 22, 2026 · Increased rate of out-of-specification endotoxin results. - Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015. recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported April 22, 2026 · Increased rate of out-of-specification endotoxin results. - Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710. recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported April 22, 2026 · Increased rate of out-of-specification endotoxin results. - Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505. recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported April 22, 2026 · Increased rate of out-of-specification endotoxin results. - ARTIS Pheno VE30A and VE40A recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported April 22, 2026 · During 3D acquisitions, lighter and darker patient images may be captured, which may result in less accurate 3D reconstruction. The variation of brightness is... - Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only recall (Wilson-Cook Medical Inc.)
Medical deviceClass IIReported April 22, 2026 · Due to increased in complaints their is the potential for endoscopic clipping device to malfunction. - Arjo Tenor mobile passive patient lift recall (ARJOHUNTLEIGH POLSKA Sp. z.o.o.)
Medical deviceClass IIReported April 22, 2026 · An internal component of the actuators in a certain production batch may not meet the required mechanical strength. This could result, in the worst case... - LinkBio CORE Workstation recall (Linkbio Corp.)
Medical deviceClass IIReported April 22, 2026 · The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen. - Yeastone Broth recall (Remel, Inc)
Medical deviceClass IIReported April 22, 2026 · Products may report incorrect AST results during quality control. Health consequences may include delayed response or the need to change to another antifungal... - Philips AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medical device recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 22, 2026 · Potential safety issue involving the Mean Aneurysm Flow Amplitude (MAFA) ratio of AneurysmFlow (Interventional Tool). Philips has determined that the MAFA... - B Braun Hemodialysis Bloodlines recall (B Braun Medical Inc)
Medical deviceClass IReported April 22, 2026 · Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. - B. Braun Hemodialysis Bloodlines recall (B Braun Medical Inc)
Medical deviceClass IReported April 22, 2026 · Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. - B. Barun Hemodialysis Bloodlines recall (B Braun Medical Inc)
Medical deviceClass IReported April 22, 2026 · Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. - B. Braun Hemodialysis Bloodlines recall (B Braun Medical Inc)
Medical deviceClass IReported April 22, 2026 · Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. - B. Braun Hemodialysis Bloodlines recall (B Braun Medical Inc)
Medical deviceClass IReported April 22, 2026 · Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. - B. Braun Hemodialysis Bloodlines recall (B Braun Medical Inc)
Medical deviceClass IReported April 22, 2026 · Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. - Omnipod 5 Pods. Model/Catalog number: PT-001662 ASM 5PK Pod STRL OPS G6G7 recall (Insulet Corporation)
Medical deviceClass IReported April 22, 2026 · Due to a manufacturing defect, certain Omnipod 5 Pods from 49 lots have an internal soft cannula tear that results in insulin leaking into the Pod instead of... - Fresh Cantaloupe recall (AYCO FARMS INC)
FoodClass IReported April 15, 2026 · Potential Salmonella Contamination - Vital Nutrients Aller-C recall (Blueroot Health, Inc.)
FoodClass IIReported April 15, 2026 · Contains undeclared egg, soy, and hazelnut - Riverence Smoked Trout Dip recall (Riverence Provisions LLC)
FoodClass IIReported April 15, 2026 · Label declares cream cheese but does not declare milk - Crab Cakes various sizes sold to food service recall (Connecticut Crab Company LLC)
FoodClass IIReported April 15, 2026 · May be temperature abused, which may result in growth of Clostridium botulinum - Red Bull Extreme Male Enhancement Supplement recall (Pure Vitamins and Natural Supplements, LLC)
FoodClass IReported April 15, 2026 · FDA analysis revealed the presence of undeclared sildenafil - Blue Bull Extreme Male Enhancement Supplement recall (Pure Vitamins and Natural Supplements, LLC)
FoodClass IReported April 15, 2026 · FDA analysis revealed the presence of undeclared sildenafil - Boner Bears Honey Male Enhancement 100% Wildflower Honey recall (Pure Vitamins and Natural Supplements, LLC)
FoodClass IReported April 15, 2026 · FDA analysis revealed the presence of undeclared sildenafil and Tadalafil - Zarlengo's Double Dark Chocolate Gelato packaged in 1 Gallon bucket/pail - white round... recall (Zarlengo Italian Ice)
FoodClass IIReported April 15, 2026 · Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement. - Zarlengo's Chocolate Gelato packaged in multiple sizes recall (Zarlengo Italian Ice)
FoodClass IIReported April 15, 2026 · Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement. - Zarlengo's Chocolate Chocolate Chip Gelato packaged in multiple sizes recall (Zarlengo Italian Ice)
FoodClass IIReported April 15, 2026 · Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement. - Clonidine Transdermal System recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported April 15, 2026 · CGMP Deviations: use of an unapproved raw material - Clonidine Transdermal System recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported April 15, 2026 · CGMP Deviations: use of an unapproved raw material - Clonidine Transdermal System recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported April 15, 2026 · CGMP Deviations: use of an unapproved raw material - GE Healthcare Omnipaque recall (GE Healthcare Ireland Limited)
DrugClass IIReported April 15, 2026 · Presence of particulate matter - GE Healthcare Omnipaque recall (GE Healthcare Ireland Limited)
DrugClass IIReported April 15, 2026 · Presence of particulate matter - Xanax XR recall (Viatris, Inc.)
DrugClass IIReported April 15, 2026 · Failed Dissolution Specifications - Artificial Tears Lubricant Eye Drops recall (Preferred Pharmaceuticals, Inc.)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility - Vancomycin HCL recall (Fagron Compounding Services)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port - Vancomycin HCI recall (Fagron Compounding Services)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port - Vancomycin HCI recall (Fagron Compounding Services)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port - norepinephrine Bitartrate recall (Fagron Compounding Services)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port - norepinephrine Bitartrate recall (Fagron Compounding Services)
DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port