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Product sold without market authorization. Affected lots are labelled with unauthorized claims.

The sterility is out of specification in the affected lot (Periodic Media Fill Validation failure).

Voluntary recall-interim order authorization not approved.  Recall start date: December 2, 2021

Voluntary recall-interim order authorisation not approved. Recall start date: December 2, 2021

Voluntary recall- interim order authorisation not approved. Recall start date: December 2, 2021

On June 14, 2022, the manufacturer Fresenius Medical Care Ag & Co. Kgaa notified Fresenius Medical Care Canada, Inc. that during regular quality inspections of Aquac Uno H devices, it was discovered that the internal ethernet cable had not been…

During internal product/process review (April 2022), it was discovered that there is a potential for the core diameter to be undersized, which may lead to the router breaking. To date, Stryker has not been made aware of any adverse events related to this…

1. Difficulty separating stylet from needle, which could result in inadvertent removal of the entire needle assembly or inability to remove the stylet from an indwelling intraosseous needle, both resulting in functional loss of intraosseous access. 2.…

Zimmer GmbH is conducting a medical device field safety corrective action (removal) for one lot of the NCB femoral screws. The product in scope is part of a mix-up with a NCB humeral screw that differs in dimensions and therefore it has been decided to…

Abbott is notifying customers of the potential for programmer software (Merlin pcs) and remote monitoring software applications (Merlin.net) to display overestimated predicted battery longevity for certain pacemakers. Pacemaker/battery functionality,…

The Benzalkonium Chloride assay is out of specification in the affected lot.

The dissolution for vitamin D3 is out of specification in the affected lot.

The products may contain undeclared ingredients which are listed on the Prescription Drug List.

During a specific servicing activity, if the wrong screws are removed by the service personnel without the appropriate table supports in place, there is the potential for the table to drop. Recall start date: June 6, 2022

This recall is to inform of a potential for falsely elevated hemoglobin %A1C and hemoglobin A1C patient results to be generated using the architect hemoglobin A1C assay when analyzing whole blood or hemolysate samples with poor sample integrity, due to…