Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,324 recalls, newest first · Checked 2 minutes ago
Canada
United KingdomUltra Violette Lean Screen SPF50+ recall
The product has failed SPF testing with variable results, placing consumers at risk of sunburn.Eternaâ„¢ Implantable Pulse Generator
Abbott is notifying customers of a potential issue affecting Eternaâ„¢ spinal cord stimulation (SCS) implantable pulse generators (IPGs), Model 32400.Zenition 50
Philips has been notified by a supplier about an issue affecting integrated chips used in the image intensifier television (IITV) of the Zenition 50 systems.ICU Medical Burette Set (Clave, Shut-Off)
ICU Medical has identified a lot-specific issue where the burette component of the IV set is missing an internal shutoff valve intended to stop fluid flow.
United StatesNoxbox LTD recalls NOxBOXi Nitric Oxide Delivery System
The unexpected internal fault / system diagnostic error to result when a rapid succession of button selections is made to the user interface without waiting for the…LeMaitre Vascular, Inc. recalls Artegraft Collagen Vascular Graft. Model/Catalog/Part Numbers: AG630M
Devices were distributed with incorrect label without CE and UKCA mark, missing patient leaflet and patient implant card.FUJIFILM Healthcare Americas Corporation recalls FDR Visionary Suite
It was found that the shaft for mounting the X-ray tube unit on the support may break.Fresenius Medical Care Holdings, Inc. recalls Optiflux¿ High Flux E-beam Dialyzer Model Numbers:
To provide further information to the user to ensure proper use of the medical device.Beckman Coulter Inc. recalls SYNCHRON Systems Phosphorus
Specific SYNCHRON Systems Modular Chemistry Phosphorus (PHOSm REF 467868) reagent lots may fail calibration before the lot expiration date which causes a delay in…Inpeco S.A. recalls FlexLab and 1 more products
The FlexLab System Sample Integrity Module (SIM) includes function that determines the hemolysis, icterus, and lipemia (HIL) in blood samples.ImaCor Inc. recalls ClariTEE Miniaturized TEE probe. Model Number: CLT-010. Ultrasound miniaturized TEE…
Production assembly error resulting in the potential for reversed articulation, where moving the lever forward caused the probe tip to anteflex rather than retroflex…Applied Medical Technology Inc recalls NutraGlide Nasal Feeding Tube with Stylet and ENFit and 3 more products
The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.Corneat Vision, LTD. recalls CorNeat EverPatch and 1 more products
Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.Abiomed, Inc. recalls Automated Impella Controller
Potential cybersecurity vulnerabilities related to the operating system in the Automated Impella Controller (AIC).GE Medical Systems, SCS recalls AW Server 2.0
Firm has identified a security vulnerability in AW Server products.B Braun Medical Inc recalls PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. and 12 more products
Potential for the lid of the catheter connector to be in the incorrect position.Canon Medical System, USA, INC. recalls This device is a digital radiography/fluoroscopy system used in a diagnostic and…
It has been found that when SPOT Fluoro is first turned on, the default ROI is selected and the collimator blades move to the boundary of the ROI, and the static image…CareFusion 303, Inc. recalls BD Alaris Pump Infusion Sets for the following reference numbers: C24101E
Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and…Noxbox LTD recalls NOxBOXi Nitric Oxide Delivery System
Fluctuations may be more likely to occur if the total flow through the device sensor (used by the device to determine flow) is less than the minimum device requirement…Dr. Reddy's Laboratories, Inc. recalls Succinylcholine Chloride Injection
Out-of-Specification (OOS) result during the 6-month stability testing; decreased preservative concentration.Accord Healthcare, Inc. recalls Levothyroxine Sodium Tablets
Subpotent: During long term stability testing of Levothyroxine Sodium Tablets USP for 88 mcg, the assay content was observed below the approved specification range.RC Outsourcing, LLC recalls Bevacizumab 1.75 mg/0.07 mL
Lack of assurance of sterility.Acuity Specialty Products, Inc. recalls Wyandotte and 1 more products
cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not…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.