Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 17 minutes ago
United StatesJB Chemicals and Pharmaceuticals Ltd recalls Enalapril Maleate Tablets
Failed Impurities/Degradation Specifications:Out of specification result occurred in Organic Impurities TestAcella Pharmaceuticals, LLC recalls NAPROXEN ORAL SUSPENSION
Chemical contamination; presence of lead and lithium above specificationAjanta Pharma Ltd. recalls Duloxetine Delayed-Release Capsules and 2 more products
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.CareFusion 213, LLC recalls BD PurPrep and 1 more products
Lack of assurance of Sterility: potential product contaminationCentral Admixture Pharmacy Services, Inc (CAPS) Los Angeles recalls TPN bag
Incorrect Product Formulation: product did not contain insulin as listed in the label.
CanadaUnauthorized sexual enhancement products may pose serious health risks (March 21, 2023 to May 27, 2024)
Health Canada is advising about unauthorized sexual enhancement products that may pose serious health risks.Nitrous Oxide Chargers: Sold for Inhalation Without Market Authorization (DIN)
The affected products are sold for inhalation without market authorization (DIN) in Canada.GHK-Cu & BPC-157 powder: Unauthorized active pharmaceutical ingredients
Products sold are unauthorized active pharmaceutical ingredients (APIs).TCNâ„¢ and CSK Reusable RF electrodes
Boston Scientific has determined that the TCN™, and CSK reusable RF electrodes may not consistently meet the expected performance levels throughout the specified 20…Azurion Systems
Philips has identified that the float tabletop control on the control module of Azurion systems may experience mechanical wear over time.Stay safe when buying health products online
As part of Operation Pangea XVIII —an international effort led by INTERPOL to disrupt the online sale of counterfeit and other illegal health products around the…Azurion and Allura Xper Systems
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage.MOSAIQ
When using Anatomical Position Monitoring (APM) during a Comprehensive Motion Management (CMM) unity treatment delivery, if the user performs a baseline shift (BLS)…Bard SILASTIC® Foley Catheter
BD has received complaints, and confirmed through internal inspection that stains are present on the surface of the affected SILASTIC® catheters.Sperti™ Vitamin D Lamp
The Spertiâ„¢ Vitamin D lamp requires a medical device licence to be sold in Canada.M Zn-Air Battery Pak
The non‑tamperproof battery door in the M Zn‑Air Battery Pak (CI‑5501) does not meet IEC 60601‑1‑11:2015 clause 8.5.2 because it allows battery access without a tool…Zimmer, Inc. recalls Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and Spatula…
Ten complaints have been received identifying issues at the time of use related to the package seal, including incomplete seals, wrinkles in the seals or peeling seals.Clinical Innovations, LLC recalls Brand Name: Kiwi Omni Vacuum Delivery System Product Name: Kiwi Omni Vacuum Delivery…
Due to complaints of device breakage at the traction force gauge to handle joint.Siemens Healthcare Diagnostics Inc recalls epoc BGEM BUN Test Card
Use of the affected product can result in discrepant low pH and measured Total Carbon Dioxide (mTCO2) results and corresponding calculated values in arterial, venous…Immuno-Mycologics, Inc recalls Immy
Neutralization Buffer may contain contaminantsMerit Medical Systems, Inc. recalls Philips Bridge Prep Kit REF: K12-09098B Sterile EO and 1 more products
catheter may experience resistance when being advanced over the guidewireHealthmark Industries Co., Inc. recalls Mesh Style Tip Protectors CSW-03-2.0 Open-end style CSW-04-4.0 Closed-end style
Product does not have FDA clearance.Advanced Bionics, LLC recalls Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak…
The non-tamperproof battery door supplied with the sound processor fails to conform to IEC 60601-1-11:2015 by not requiring the use of a tool to replace the button/coin…A little guidance
Get more from your tools
Practical guide 3 min read
Recall classes explained: Class I, II and III
What the FDA's recall classes, Canada's classes and types, and UK and EU alert levels mean, with how often each one comes up.
Practical guide 3 min read
How to check if your car has a recall
Find the recalls for your make and model, confirm with your VIN whether your car is affected, and know what do-not-drive and park-outside warnings mean.
Practical guide 3 min read
What to do if something you own is recalled
Refunds, repairs, replacements and proof of destruction: what to expect, and how to handle recalled food, medicines, batteries and children's products safely.