Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
225 recalls match · Clear filters · Checked 4 minutes ago
United States
CanadaSanofi-Aventis Canada Inc. recalling certain insulin pens and cartridges
Sanofi-Aventis Canada Inc.Amplatzerâ„¢ Amuletâ„¢ Left Atrial Appendage Occluder
The current Amulet™ IFU contains a contraindication against use "where placement of the device would interfere with any intracardiac or intravascular structures."…PERMA-HAND™ Silk Suture
Ethicon determined that PERMA-HANDâ„¢ Silk Suture subject to this recall (removal) was incorrectly manufactured with an alcohol-based tubing fluid in the primary packaging.Medical Action Industries, Inc. 306 recalls Blood Culture Collection Venipuncture Kit 20/Cs
Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise…Mirion Technologies (Capintec), Inc. recalls Captus 4000e Thyroid Uptake System
Potential for failure of the tension bolt which would allow the spring arm to unexpectedly fall to its lowest position, which is approximately 25 inches (63.5 cm) from…Howmedica Osteonics Corp. recalls AXLE PIN ASSY LARGE ELBOW COBALT CHROME Catalog No. C-M112-2-500 Orthopaedic implant… and 11 more products
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years.
Schwarzkopf Professional Osis Grip Mousse recalled due to injury hazard
The recalled product has packaging issues, which can cause the product to leak from the package when under pressure.SIGNAâ„¢ Artist and SIGNAâ„¢ Artist Evo
GE Healthcare has become aware of an exposed sharp edge inside the SIGNA™ Artist Evo and SIGNA™ Artist electronics cabinet that could damage power cables, which may…
AustraliaSalon de Pro unscented hair colour fast dye cream recall
The warning label on the product is unclear, is in the wrong position and does not comply with regulatory requirements.Mise en scéne Hello Bubble Foam Hair Colour recall
The warning label on the product is unclear, is in the wrong position and does not comply with regulatory requirements.Kao Liese Prettia Bubble Hair Colour recall
The warning label on the product is unclear, is in the wrong position and does not comply with regulatory requirements.RAPICIDEâ„¢ PA High Level Disinfectant
STERIS identified through customer complaints that a small number of RAPICIDEâ„¢ Part A bottles within certain lots may begin to bulge or expand over time.IntelliSpace Critical Care And Anesthesia
In ICCA releases J.06.01 and J.06.02, calculations triggered by infusion-pump auto-charting may result in incorrect Intake Totals, Output Totals, Net Body Balance…NDI Passive Spheres™
The sphere manufacturer has identified variation in the reflective material used on a limited number of sterile passive sphere lots.Given Imaging Ltd. recalls Bravo CF capsule delivery device
Capsule may fail to attach to the esophagus or detach from the delivery device.Coloured contact lenses designed for cosplay and makeup applications recall
The packaging solution for these contact lenses may be contaminated with Burkholderia cepacia complex bacteria.
Generic acetaminophen by Teva recalled because it may contain foreign material
Teva Canada Limited is recalling one lot of the non-prescription drug Novo-Gesic Forte 500 mg (acetaminophen) due to the potential presence of phenolic resin or epoxy…Medline Industries, LP recalls Medline Convenience Kits: 1) DRAWER 9 CRICOTHYROTOMY KIT and 15 more products
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper…Adora Pecker Finger vibrator recall
The product’s USB charging cable may short circuit and overheat and/or catch fire while connected to any USB power source.
Traditional Kohl Products recalled due to chemical hazard
The recalled products contain lead above the impurity limits outlined in the Guidance on Heavy Metal Impurities in Cosmetics.LIFEPAK ® 35 Monitor/Defibrillator
Stryker has identified an issue with the LP35 where the device does not display the message "CHECK RHYTHM / ECG Analysis Inconclusive" as intended when specific…IMRIS Imaging Inc recalls ORT200 and 1 more products
The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked…Med-Rx Medication/Primary Solution Administration Kit
CHS was notified by ICU Medical Canada that they are conducting a recall of certain IV sets as discoloration may be present in the drip chamber of the IV sets.A little guidance
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