Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 19 minutes ago
United States
CanadaOctreotide for injectable suspension; Good manufacturing practices concerns
Quality concerns of affected lots due to deficiencies in Good Manufacturing Practices (GMP).
Teva Octreotide for injectable suspension recalled due to potential drug quality issues
Teva Canada Limited is recalling all strengths (lots listed above) of the prescription drug Octreotide as a precautionary measure due to deficiencies in Good…Locametz powder for solution, kit; Out of specification (unknown impurity)
An unknown impurity is out of specification in the affected batch.
Fake Cialis and Viagra seized from Bitco Distribution in Ontario
Health Canada has seized counterfeit Viagra and Cialis from Bitco Distribution in Mississauga, Ontario.
The Paris Apothecary Aristocrat Beard Oil and Beard Balm recalled due to a chemical hazard
Health Canada’s sampling and evaluation program has determined that the recalled products contain methyl eugenol above the maximum concentration outlined in the…
United KingdomBajaj Almond Drops Hair Oil safety warning
The product presents a serious chemical risk as it contains butylphenyl methylpropional, also known as lilial or BMHCA.BS 3/8x3/32 L1.7 (Bubble Sensor for 3/8” X 3/32” tubing, length 1,7 m)
Internal investigations have identified an issue with the durability of the connecting cable near the connection to the Bubble Sensor.Sheathing Technologies Inc recalls Sheathes3D Seamless Viral Barrier
Vaginal/rectal ultrasound probe covers with a viral barrier may have product defects, which may result in contamination during use, posing an infection risk.Shenzhen Atomstack Technologies recalls Material Processing Laser Products
Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)Ferndale Laboratories, Inc. recalls Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive Model/Catalog Number…
Butyrate tube cracks during actuation, rendering product unusable.Philips Ultrasound, LLC recalls Philips EPIQ Ultrasound Systems
Retroactive: Ultrasound may experience an unexpected automatic reboot, resulting in damage to transducer.Vortex Surgical Inc. recalls Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe
Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.Beaver-Visitec International, Inc. recalls BVI Leos Laser and Endoscopy System. Model Number: OME6000U.
Manufacturing deviation in which the ferrites specified for the USB cable assembly linking the Nurse Monitor touchscreen to the System Controller were not installed as…CareFusion 213, LLC recalls BD ChloraPrep" Triple Swabsticks
Lack of Assurance of SterlityNovo Nordisk Inc. recalls Wegovy and 1 more products
Presence of Particulate Matter: Hair was found in a prefilled syringeGlenmark Pharmaceuticals Inc., USA recalls Ondansetron Orally Disintegrating Tablets
Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets falling out.Zydus Pharmaceuticals (USA) Inc recalls traZODONE Hydrochloride Tablets
Failed Tablet/Capsule Specifications: Product complaint received that some tablets had a dent on the plain side of the tablet surface.Cardinal Health™ Chest Drain Units and Accessories
The purpose of this action is to communicate to customers that the instructions for use (IFUs) on the listed Cardinal Health Chest Drainage Units (CDUs) and Accessories…Allura Xper and Allura CV20 Systems
Philips has identified a potential safety issue in certain Philips Allura Xper and Allura CV20 Systems that have a Laird cooling unit installed which may result in a…Jumper Medical Fetal Doppler
Health Canada has identified potential risks when fetal dopplers are used at home without professional supervision.JAMP-ASA 81 mg EC; Out of specification (salicylic acid impurity)
The impurity, free salicylic acid, may be out of specification in the affected lot.Patient Information Center IX
Philips has become aware of a potential safety issue concerning PIC IX 4.5.0 default mobile event notification filters change.ShockPulse Lithotripsy System, Generator and Transducer
Olympus has identified instances of ShockPulse generator remaining in a blinking phase waiting to recognize the transducer following previous FY26-010 recall.A little guidance
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