Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,312 recalls, newest first · Checked 20 minutes ago
United StatesINSPIREMD Inc recalls Brand Name: CGuard¿ Prime Carotid Stent System and 5 more products
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.Golden State Medical Supply Inc. recalls GSMS Incorporated
Failed Dissolution Specifications: During 12-month long-term stability testing, subject lot was out of specification (low) for stage 3 dissolution at the 24-hour…Amneal Pharmaceuticals, LLC recalls Primidone Tablets
Cross Contamination with Other Products: due to a potential for cross-contamination with Acemetacin API due to an issue at the API manufacturer.Sun Pharmaceutical Industries Inc recalls DOXOrubin Hydrochloride Liposome injection
Presence of Particulate matter: Particulate matter identified as glass.Fresenius Kabi USA, LLC recalls Epinephrine Injection
Failed Impurities/Degradations SpecificationsBreckenridge Pharmaceutical, Inc. recalls Duloxetine Delayed-Release Capsules and 1 more products
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limitZep Inc recalls Zep
Microbial contamination of sterile productsSun Pharmaceutical Industries Inc recalls Budesonide Inhalation Suspension
Presence of Foreign Substance:This recall has been initiated in response to a product quality complaint reported for black/brown specs and particles within the ampoule…Beekeeper's Naturals USA Inc. recalls BEEKEEPER'S NATURALS Saline Nasal Spray
Microbial Contamination of Non-Sterile ProductsHaleon US Holdings LLC recalls Gas-X Extra Strength
Chemical Contamination: contamination with a diluted propylene glycol-based coolant from a machine leakage during the packaging process.Ascend Laboratories, LLC recalls Minocycline Hydrochloride Extended-Release Tablets
Failed Dissolution Specifications: An out-of-specification (OOS) result was observed during the 9th month of dissolution test analysis
CanadaLancora Tablets; Broken / partial tablets in blister pack
Presence of partial tablets in the blister packs.Unauthorized soft-shelled hyperbaric chambers may pose serious health risks 2026-06-16
Health Canada has received several complaints related to the use of unauthorized soft-shelled hyperbaric chambers and they are increasingly found in wellness centres in…GE Healthcare Integrated and Stand-Alone Resuscitation systems
GE HealthCare has become aware of a potential issue involving the air-oxygen blender knob shaft on certain (serial number specific) integrated and stand-alone…ETMS 70 mm Cooled Coil
A potential issue manifests as an electrical arc within the coil itself that, when occurs, leads to a relatively loud popping sound, which can startle the patient or…Aptima HIV Quant Dx Assay, HCV Quant Dx Assay, and HBV Quant Assay Software
This notification is to inform Panther and Panther Fusion users that assay installer (version 2.0.0.9) including the Aptima HIV Quant Dx Assay, HCV Quant Dx Assay, and…Selenia Dimensions 2D/3D Mammography Systems
Hologic is initiating this voluntary field safety corrective action because the vertical travel assembly on 3Dimensions and Selenia Dimensions systems may experience…Nicotine Pouch Recall; No market authorization
Product sold without market authorization (DIN) in Canada.
CannaPiece Corp. recalls Wild West 96+ Strawberry Stampede Liquid Diamonds 510 Vape due to a labelling issue
The label for the affected product has incorrect cannabinoid values.Baxter Healthcare Corporation recalls Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number…
Affected lots may contain incorrect 0.8-micron filters.Fresenius Kabi USA, LLC recalls Ivenix Infusion System
Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components that may not be…Windstone Medical Packaging, Inc. recalls Aligned Medical AMS16835 Fluids Kit RX
Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.Fresenius Kabi USA, LLC recalls LVP software of the Ivenix Infusion System
Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut down the…A little guidance
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