Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,304 recalls, newest first · Checked 9 minutes ago
Canada
United StatesPar Health Issues Voluntary Nationwide Recall of Two Lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection Due to the Presence of Particulate Matter
Presence of particulate matter identified as cellulose or stopper material
Counterfeit laser hair removal and therapy devices found in some clinics and may pose serious health risks
Health Canada is advising Canadians about counterfeit laser hair removal machines and therapy systems sold under the “Soprano” brand.SIGNA™ Artist and SIGNA™ 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.RAPICIDE™ PA High Level Disinfectant
STERIS identified through customer complaints that a small number of RAPICIDE™ Part A bottles within certain lots may begin to bulge or expand over time.Trinity Biotech Oxalate Reagent Kit
Trinity Biotech is recalling Oxalate Reagent B, Product Code 591-2, Lot 2500711 due to performance variability resulting in negative bias and under-recovery of oxalate…Philips Ingenia, Achieva and Intera MR Systems
When exporting diffusion tensor imaging (DTI) scans from a Philips MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion…
Otsuka ICU Medical LLC Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection, USP Due To a Product Mix-up with 10 mEq Potassium Chloride Injection
Product mix-up where 0.9% Sodium Chloride Injection, USP overwrap may contain 10 mEq Potassium Chloride Injection
United KingdomBaylis & Harding Oud, Cedar & Amber 1L Hand Wash Refill recall
The product presents a microbiological risk as testing identified the presence of Pluralibacter gergoviae.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.Platinum Naturals Easymulti Stress (men): Affected lots incorrectly labelled for Vitamin B6 quantity
Affected lots are labelled with the incorrect amount of a medicinal ingredient (Vitamin B6).Given Imaging Ltd. recalls Bravo CF capsule delivery device
Capsule may fail to attach to the esophagus or detach from the delivery device.AVID Medical, Inc. recalls Halyard IV Start Kit Non-Sterile REF: KRIV26-02
Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may…Medical Action Industries, Inc. 306 recalls Kit: Epidural/Pain TQC 20/Cs and 1 more products
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.Windstone Medical Packaging, Inc. recalls AMS Convenience Kit: DSAEK Pack
The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that have…HeartSine Technologies Ltd recalls HeartSine SAM 350P 350P US Device
Due to a damaged (over stretched) membrane tail that causes an intermittent fault.Atrium Medical Corporation recalls Getinge PVC Thoracic Catheter and 2 more products
An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.C.R. Bard Inc recalls Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF… and 5 more products
Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.Lutronic Corporation recalls Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser device that…
Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in patient burn.Nipro Renal Soultions USA, Corporation recalls MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201 and 3 more products
Hemodialysis concentrates contain high endotoxin levelsA little guidance
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