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Displaying 1 - 15 of 3547 items.

Health alert or recall Signa, Discovery and Optima Products
GE Healthcare (GEHC) MR systems could potentially have a cryogen ventilation system that does not meet the venting requirements. Failure to have proper venting could present a safety issue if the cryogen gas is vented into the MR room during a magnet…
RecallHealth product recall | 2022-01-18
Health alert or recall Signa Products
GE healthcare (GEHC) MR systems could potentially have a cryogen ventilation system that does not meet the venting requirements. Failure to have proper venting could present a safety issue if the cryogen gas is vented into the MR room during a magnet…
RecallHealth product recall | 2022-01-18
Health alert or recall Arrow-Trerotola Products
Teleflex is initiating a voluntary field safety corrective action due to reports received indicating PTD tip separation during use. If the tip separates during use, clinicians may exercise their medical judgment to either retrieve endovascularly with a…
RecallHealth product recall | 2022-01-18
Health alert or recall PAXLOVID (nirmatrelvir and ritonavir) - Dosing and Dispensing in Renal Impairment, Risk of Serious Adverse Reactions Due to Drug Interactions, and English-Only Labels
PAXLOVID (nirmatrelvir and ritonavir) was authorized by Health Canada on January 17, 2022. PAXLOVID is not recommended in patients with severe renal impairment and requires a dosage reduction in patients with moderate renal impairment. PAXLOVID may also…
AlertHPRC | 2022-01-17
Health alert or recall Endurant Iis Stent Graft System
Devices built with specific batches of taper tip assemblies have the potential for the taper tip to detach from the delivery system. Detachment of the taper tip during the implant procedure may lead to a secondary intervention to attempt to remove the…
RecallHealth product recall | 2022-01-17
Health alert or recall Piperacillin and Tazobactam for injection: Particulate
Visible particles observed in vials following reconstitution 
RecallHealth product recall | 2022-01-17
Health alert or recall Batec Mobility Products
Loss of some brake disc bolts was detected. Possible cause is that the screws were not tightened properly. Recall start date: Jan 3, 2022
RecallHealth product recall | 2022-01-17
Health alert or recall Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 15 Mm, 83 Mm Long
Zimmer Biomet is conducting a lot specific medical device recall for the comprehensive shoulder system mini humeral stem. The products in scope underwent an incorrect rework operation for the porous plasma sprayed coating. Internal testing indicated that…
RecallHealth product recall | 2022-01-17
Health alert or recall Optima Mr430s 1.5t - Main Unit
GE healthcare (GEHC) MR systems could potentially have a cryogen ventilation system that does not meet the venting requirements. Failure to have proper venting could present a safety issue if the cryogen gas is vented into the MR room during a magnet…
RecallHealth product recall | 2022-01-17
Health alert or recall Bd Veritor Plus Analyzer
Bd has received two (2) complaints reporting that the Bd Veritor Plus analyzer may have the potential to overheat and/or cause fire. Bd's investigation has found that the issue can occur when an unauthorized alternative ac power adapter, and not the one…
RecallHealth product recall | 2022-01-17
Health alert or recall Somatom Edge Products
Decreased head image quality on P46 systems after VB20 SP5 installation. This customer advisory notice provides a detailed error and workaround description. Recall start date: Jan 6, 2022
RecallHealth product recall | 2022-01-17
Health alert or recall Syngo.Via
An issue observed when creating a new GLM series with MOCO (motion correction) and /or spatial filtering using the MR Neuro 3D calculation in the MR Neuro3d workflow. Recall start date: Jan 6, 2022
RecallHealth product recall | 2022-01-17
Health alert or recall Crag Lateral Flow Assay
The devices were found to have reduced specificity (90% now versus 99% before). Recall start date: Jan 3, 2022
RecallHealth product recall | 2022-01-17
Health alert or recall Health Canada safety review finds link between the use of Xeljanz and Xeljanz XR (tofacitinib) and increased risk of serious heart-related issues and cancer
UPDATE - January 12, 2022: Safety Review found a link between the use of Xeljanz/Xeljanz XR (tofacitinib) and the risks of serious heart-related problems and cancer Health Canada completed a safety review that confirmed a link between the use of…
AlertPublic advisory | 2022-01-12
Health alert or recall XELJANZ/XELJANZ XR (tofacitinib) – Risk of Major Adverse Cardiovascular Events, Malignancy, Thrombosis and Infection
A post-authorization safety study in RA patients 50 years of age or older with at least one additional CV risk factor showed an increased risk of MACE and malignancy in patients treated with XELJANZ (5 mg BID or 10 mg BID) in comparison to TNFi. An…
AlertHPRC | 2022-01-12
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