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
SPECTRALIS® with Flex Module
There is a possibility that the castor wheels of the Flex stand are not properly attached.Embosphere® Microspheres-Syringe
Merit Medical Systems, Inc., on behalf of its subsidiary, Biosphere Medical, is voluntarily recalling specific lots of the Merit Embosphere® Microspheres due to a…Two lots of Teva-Pregabalin 150 mg capsules recalled due to cross-contamination with the drug sertraline
Teva Canada Ltd.Orthopaedic Implant Components
Stryker has become aware that the devices listed in the Customer Letter were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in…Siemens Healthcare Diagnostics, Inc. recalls Syva Emit Disopyramide Assay Enzyme Immunoassay
Out-of-specification sodium azide concentration in Syva Emit Disopyramide Enzyme Immunoassay Calibrator Lot U1.Boston Scientific Neuromodulation Corporation recalls INFINION CX LEAD KIT
Spinal cord stimulation system lead body may be exposed to stress at the anchor site.Munevo GMBH recalls munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control…
A software issue may cause the wheelchair's driving mechanism to fall out of calibration.Pride Mobility Products Corp. recalls Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum… and 12 more products
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use.Siemens Healthcare Diagnostics, Inc. recalls Syva Emit tox Serum Tricyclic Antidepressant Calibrator/Controls SMN 10445390 Catalog…
out-of-specification sodium azide concentration in Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls Lot U2.Bravo - Capsule Delivery System
Medtronic has identified an increase in complaints involving the Bravo CF capsule delivery device where the capsule fails to attach to the esophagus or detach from the…RELLET Hyaluronic Acid Deep Hydrating Spray recalled due to missing mandatory hazard labelling
The recalled products do not have mandatory hazard labelling as required by the Cosmetic Regulations under the Food and Drugs Act.Permobil Inc recalls Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031
This recall has been reported retroactively.Medtronic Perfusion Systems recalls EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR and 5 more products
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass.Karl Storz Endoscopy recalls Flexible Hystero-Fiberscope Kits REF: 11264BBU1
Flexible hysteroscopes indicated for use during diagnostic and operative hysteroscopic procedures may contain an expired single use endoscopic seal for gynecology use…Penumbra, Inc. recalls Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT
Due to manufacturing issues, reperfusion catheters may fracturesGE Medical Systems, LLC recalls Optima XR200amx and 2 more products
GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may…Atellica® CH Urine Albumin (UAlb)
Siemens Healthineers has confirmed, through the investigation of customer complaints, the potential for the following issues associated with processing Atellica CH…Cardiac Workstation
The cardiac workstation can intermittently provide inaccurate data related to the patient's native heart rate.Biomerieux Inc recalls VITEK 2 AST-N447 TEST KIT Product reference 424620
Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures.Phantom® Hindfoot TTC/TC Ball Tipped Guide Rod
Zimmer Biomet Canada on behalf of Paragon 28, Inc.Allura Xper FD10
Philips has identified through customer complaints that, during certain repair or service actions, Hard Disk Drives (HDD) with different performance characteristics…Medacta Usa Inc recalls Short Monobloc Stem Broaches
Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the stem…Accuray Incorporated recalls Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console.A little guidance
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