Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,304 recalls, newest first · Checked 26 minutes ago
CanadaV-Locâ„¢ 90 and 180 Suture Products
On 29-Jan-2026 during a quality inspection at a manufacturing site, a V-Loc 180 unit was found with a hole in the breather pouch on the Tyvek side.SEMA 3
When an ECG is aquired with DEFIGARD Touch 7 or ARGUS PRO LifeCare 3 with the newest software, there might be a discrepancy between the aquiring device and SEMA.StrykeFlow PS and AHTO
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.Philips Allura Xper FD series
Philips has identified a potential safety issue affecting Allura R8.2 systems equipped with a AD7x patient table type potentially leading to loss of geometry movements.Cardiac Workstation
The cardiac workstation can intermittently provide inaccurate data related to the patient's native heart rate.Leoni Plus
An electronic component may overheat internally.Presource ®Kits containing Teleflex Pilling® Wecksorb Neurosponge
Cardinal Health was recently informed of a medical device recall from Teleflex concerning the Pilling® Wecksorb Neurosponge referenced.CTP - Tubing sets
The manufacturer became aware of this issue due to six customer complaint reports.Supernova and Supreme Nicotine Film and Pouches Recall; No market authorization
Product sold without market authorization (DIN or NPN) in Canada.Solarâ„¢ GI
Under extended clinical use conditions (e.g., long-duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing…
United StatesIntegra LifeSciences Corp. (NeuroSciences) recalls OmniTract Surgical Retractor System
The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes.Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS and 1 more products
Due to packaging discrepancy with incorrect product size mixed up.Boston Scientific Neuromodulation Corporation recalls Intracept Access Instruments
Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if breached…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.Think Surgical, Inc. recalls TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking…
Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.Fresenius Medical Care Holdings, Inc. recalls 5008X Blood Tubing Set
Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the 5008X CAREsystem.Elekta, Inc. recalls Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote… and 2 more products
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Enzymatic Hemoglobin A1c
The potential for intermittent well-to-well bias on the A1c_E assay on the Atellica CH and Atellica CI analyzer which could cause falsely depressed or falsely elevated…Medline Industries, LP recalls Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF and 2 more products
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr.CMR Surgical Limited recalls Brand Name: Versius Surgical System US Product Name: Vesius Surgeon Console US…
Secure Boot was mistakenly not enabled at manufacturing time, which presents a potential cybersecurity risk.Olympus Corporation of the Americas recalls Olympus Single Use Distal Cover
Olympus has developed and released newly designed version of the Distal Cover (MAJ-2315) to replace previous design of the Single Use Distal Covers.Medtronic MiniMed, Inc. recalls MiniMed 780G Insulin Pump
A software anomaly can occur when the pump is paired with the Instinct sensor.Klowen Braces recalls KL Owen Custom Orthodontic Solution
A product error defect may cause incorrect bracket placement.A little guidance
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