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Displaying 1 - 15 of 3936 items.

Health alert or recall BD Vacutainer Tube Sodium Fluoride/Potassium Oxalate
The affected product ref 367001, BD vacutainer tube sodium fluoride: 100 mg, potassium oxalate: 20 mg, gray top, 10 ml contains isobutylene (also known as isobutene or 2-methylpropene) which in a recent publication demonstrated potential interference in…
RecallHealth product recall | 2022-09-28
Health alert or recall Unauthorized products may pose serious health risks
Health Canada is advising about unauthorized health products that may pose serious health risks. The table is updated when Health Canada finds unauthorized health products that are promoted for sexual enhancement, weight loss, as a workout aid, as "…
AlertPublic advisory | 2022-09-27
Health alert or recall Lumi Lash: Unlicensed product with ingredient on prescription drug list.
Product sold without market authorization (DIN) in Canada. All affected lots may contain bimatoprost, a prostaglandin analogue, which is listed on the prescription drug list.  Test results for Lot 20220331 found the product to contain bimatoprost.…
RecallHealth product recall | 2022-09-26
Health alert or recall Magnets in certain Philips Respironics sleep therapy masks may cause serious injury to some individuals
Certain Philips Respironics sleep therapy masks used with Continuous Positive Airway Pressure (CPAP) or Bi-Level Positive Airway Pressure (BiPAP) machines have magnets in their headgear clips or straps. These magnets could cause safety concerns for…
AlertPublic advisory | 2022-09-26
Health alert or recall Novum IQ Large Volume Pump
Through ongoing internal testing, Baxter Corporation has observed isolated incident of over infusion on the Novum IQ LVP infusion pump during test runs at 0.1 ml/hr after 40 hours of continuous infusion within the 96-hour set change interval. Recall…
RecallHealth product recall | 2022-09-23
Health alert or recall Respironics Masks
The affected masks contain magnets which can potentially affect the functioning and/or induce the movement/dislocation of medical implants or medical devices that can be impacted by the magnetic fields. Recall start date: September 15, 2022
RecallHealth product recall | 2022-09-23
Health alert or recall Gelita Tuft-It®
The endotoxin limit/specification appears to have been exceeded in re-testing using a new method. Recall start date: September 9, 2022
RecallHealth product recall | 2022-09-23
Health alert or recall Prismaflex Sets
Baxter Corporation is issuing an urgent medical device correction for the Prismaflex sets listed. The current Prismaflex set IFU is a single booklet containing 27 translated languages, and the following products include a mistranslation in the Estonian (…
RecallHealth product recall | 2022-09-23
Health alert or recall Mitraclip/Triclip G4 Delivery Systems
Abbott has observed an increase in complaints regarding clip locking malfunctions. Abbott is bringing awareness and taking action to emphasize the relevant steps of the instructions for use (IFU) to aid in optimal function of the clip locking mechanism.…
RecallHealth product recall | 2022-09-23
Health alert or recall Leica Microsystems M530 Optics Carrier
During internal testing Leica Microsystems has become aware of a component change on the photodiodes inside the M530 Optics Carrier. The photodiodes are used as luxmeters to optimize the "brightcare plus" limit which is calculated based on real-time…
RecallHealth product recall | 2022-09-23
Health alert or recall Alinity Hs/Hq System
The Alinity h-series system control center (SCC) application software version 4.3 (and below) and the local user interface (LUI) embedded analyzer engine (EAE) contain a cybersecurity certificate that expired on 08sep2022.  Whenever the software…
RecallHealth product recall | 2022-09-23
Health alert or recall Riva-Oxazepam: Incorrect label (Riva-Oxazepam 30MG 500 tablets DIN00568414) may be appended to affected lots that contains: Riva-Oxazepam 15MG 500 tablets DIN00568406
Incorrect label (Riva-Oxazepam 30MG 500 tablets DIN00568414) may be appended to affected lots that contains: Riva-Oxazepam 15MG 500 tablets DIN00568406. 
RecallHealth product recall | 2022-09-22
Health alert or recall Esomeprazole, Candesartan and Pravastatin Tablets: OOS result for Finished Product Assay and/or Blend Uniformity
Out of Specification result for Finished Product Assay and/or Blend Uniformity
RecallHealth product recall | 2022-09-21
Health alert or recall Venlafaxine: OOS result for Spheroids Dissolution Rate Profile (DRP)
  Out of specification result for Spheroids Dissolution Rate Profile (DRP) 
RecallHealth product recall | 2022-09-21
Health alert or recall Heat And Moisture Exchanger (HME) And Filters
Teleflex is initiating this voluntary recall for the above-mentioned products due to reports of the device splitting or detaching during use. The devices are intended for connection to respiratory equipment in intensive care units and operating theatres…
RecallHealth product recall | 2022-09-20
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