Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
225 recalls match · Clear filters · Checked 1 minute ago
United StatesTechno-Path Manufacturing LTD. recalls Techno-Path Multichem AE Unassayed Level 1 REF:AE621X and 2 more products
A routine stability studies have identified a stability drift affecting the Ammonia (NH4+) analyte in specific lots of Multichem AE quality control material.
CanadaBIOFIRE Blood Culture Identification 2 (BCID2), 30-Pack
BioMérieux has received complaints of false negative results on BIOFIRE BCID2 Panel kit lot 0727226 / pouch lot 3ZQT26 and investigation identified a product issue.Siemens Healthineers AG Magnetom and Biograph One Systems
A software issue has been identified in syngo.via MR Cardiac Analysis MR Flow Quantification affecting the evaluation of retrospectively gated 2D cardiac flow data.Steris Corporation recalls RAPICIDE PA Part A High-Level Disinfectant and 2 more products
If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure.Beckman Coulter, Inc. recalls DxU 840m Iris and 1 more products
The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however, the check…Baxter Healthcare Corporation recalls Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product…
Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift strap…ARCHITECT "I" System - i2000SR Processing Module - Class 4
An issue has been identified with the 5 Amp (5A) diode used in the Induction Heater (IH) Control Module on the ARCHITECT i2000SR IH Kit (optional hardware).cobas® c 303 analytical unit
An issue has been identified where vacuum tubing of the cell rinse unit of the cobas c 303 analytical unit prematurely deteriorated.Medline Industries, LP recalls Rollator and 1 more products
The front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing.Steris Corporation recalls VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB006 and 5 more products
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification.Cardinal Health Presource Kits
Cardinal Health Presource® has identified various kits that may contain a component impacted by the welmed, extension tubing sets component.Penumbra Inc. recalls Brand Name: Penumbra System
Due to manufacturing issues reperfusion catheters may fracture.Cardinal Health 200, LLC recalls Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT and 3 more products
The kits contain tube sets with handpieces that may leak during use.Medline Bariatric Rollator
Specific lots of Medline BariatricRollator (SKU: MDS86800XWS), are being recalled due to the front fork stem bolt/wheel assembly disconnecting from the rollator frame…Precision Pointer Electromagnetic (EM)
Stryker has identified that the tip of the Precision Pointer EM may potentially fracture at the laser welding seam.Hexavue Focus Integrated System
A software issue may result in unintended mismatch of patient information on manually printed images.Medline Sterile Surgical Kits containing Medline C-Section Drape w/Incise
A recall correction notice for Medline Sterile Surgical Kits containing Medline C-Section Drape w/Incise is being issued due to reports of the drapes being difficult to…Radiography 7000 M
Philips has become aware of a potential safety issue impacting the Radiography 7000 M system (Model 712010) where the drive function may fail immediately after an…Ethicon Nylon Suture
Ethicon determined that some ETHILONâ„¢ Nylon Suture from the lot subject to this recall (removal) have needles that are distorted/twisted in the primary packaging.Maquet SAS recalls PowerLED 300 Concealed Lighting System
The potential for the device to detach at the junction between the spring arm and suspension arm and fall causing potential injury.Boston Scientific Corporation recalls Imager II Angiographic Catheters M001314001 IMAGER II/5/ST/65/038 BX5
Tip may fracture or detach, leading to device fragments remaining within the patient or migrating through the vasculature.Heidelberg Engineering GmbH recalls Brand Name: Heidelberg Engineering GmbH Product Name: SPECTRALIS with Flex Module…
Wheels may come loose when module is being pushed or pulled during movement or transportation, affecting stability of the stand.Biomerieux Inc recalls VITEK 2 AST-N461 TEST KIT
The issue is related to card pouch damage associated with a portion of the lot which was produced on a specific card pouching device, in a specific timeframe, causing a…A little guidance
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