Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,324 recalls, newest first · Checked 0 minutes ago
CanadaPhilips IntelliVue Patient Monitors
Philips IntelliVue patient monitors provide a feature for pausing all alarms for a configured timeframe or for switching all alarms off for an infinite period until…
Expanded recall: Various Magic BM products recalled due to missing mandatory hazard labelling
These products do not meet the Cosmetic Regulations in Canada.Access 2 Reaction Vessels
Instrument testing replicated failures seen in the field (e.g., pipetting, rake, wash carousel errors) for suspect RV lots.Inlay Optimaâ„¢ Ureteral Stent Without Guidewire Kit, Length 30cm, 6Fr
BD has identified a labeling discrepancy involving Inlay Optimaâ„¢ ureteral stents based on customer complaints.BD BACTECâ„¢ MGITâ„¢ 960 PZA Kit
This a follow-up letter to previous field safety notifications IDS-24-5091/IDS-25-5091-EXP.Henry Schein Maxima Diamonds FG (Burs)
Henry Schein Inc.Tamper Evident Additive Port Cap
The recall was initiated by IMI following their internal discovery that the corrugated shipper box contains incorrect compatibility information.OraVerse: Distribution to wholesalers who do not hold an establishment license for sale of the product in Canada
Distribution of a prescription drug to wholesaler(s) who did not hold an establishment license.Hemochron® Jr. Whole Blood Microcoaguation System - ACT-LR Test Cuvette
A complaint was received from a customer about finding a foreign object (single edge blade) inside one (1) Hemochron® JACT-LR test cartridge.Septodont Products: Cracked glass cartridges
Glass cartridges may be cracked in the affected lot(s).RADspeed Pro X-Ray and CH-200, CH-200M Ceiling Tube Supports
The CH-200 and CH-200M ceiling tube supports include a suspension mechanism and rotating shaft that allow x-ray tube positioning.SLSolutionâ„¢
SLSolution™ reagent includes dithiothreitol (DTT), which is oxidized when it gets in contact with air and/or metals, potentially losing its functionality in…Quantum Intersegmental Table
This product is being recalled due to the heat function that may become damaged over time due to patients pressing on the areas with heat function components.Life Brand Magnesium Bisglycinate 200mg: Undeclared ingredient (Magnesium Oxide)
Affected lots contain an undeclared ingredient (Magnesium Oxide).
United StatesIntegra LifeSciences Corp. (NeuroSciences) recalls TruDi¿ Navigation System
It was determined that when the navigation system is configured with specific revision combinations of the Multi Instrument Adapter together with the Patient Tracker…Beckman Coulter Inc. recalls SYNCHRON Systems Direct LDL Cholesterol
Beckman Coulter has identified that there is an increased probability Synchron Systems Direct LDL Cholesterol (LDLD REF 969706) reagent lot M404166 may generate false…Tandem Diabetes Care, Inc. recalls Tandem Mobi Insulin Pump: Description/Catalog: Tandem insulin pumps are battery-operated…
Insulin pump includes a vibration motor that gives tactile feedback for any alerts, alarms, or malfunctions.Elekta, Inc. recalls Brand Name: Leksell Stereotactic System Product Name: Leksell Vantage Stereotactic…
Due to increased risk that paint flakes from the engravings may separate from the device and there is the possibility that the flake may inadvertently enter the woundSpacelabs Healthcare, Ltd. recalls Brand Name: Sentinel V11 Product Name: Sentinel V11 Model/Catalog Number: 92810 Software…
Due to two distinct issues: 1.Total Joint Orthopedics, Inc. recalls Brand Name: Klassic BiPolar Head Model/Catalog Number: 3205.41.022 Klassic BiPolar Head
Potential packaging issue that could compromise the sterile barrier.Beckman Coulter, Inc. recalls Beckman Coulter UniCel DxI 600 and 1 more products
An internal investigation has determined that due to defective sub-components within the gantry assembly, a z-axis CAD movement motion error may occur and cause an…Zimmer, Inc. recalls Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene and 1 more products
Zimmer Biomet is conducting a medical device recall for two (2) lots of the Dual Mobility Vivacit-E¿ Bearing due to a commingle.OSSTEM Implant Co., Ltd. recalls Osstem Dental X-Ray System T1. Product Model Numbers T1-C and T1-CS. and 2 more products
Osstem Implant Co.A little guidance
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