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Displaying 1 - 15 of 59 items.
United Wings Enterprise Inc. recalls COVID-19 Preventive Prescription products sold without market authorization and unauthorized claims.
Product sold without market authorization. Affected lots are labelled with unauthorized claims.
RecallHealth product recall | 2022-06-30
Dr. Reddy's Laboratories Canada Inc. recalls a lot of Succinyl Choline Injection USP
The sterility is out of specification in the affected lot (Periodic Media Fill Validation failure).
RecallHealth product recall | 2022-06-30
Defigard Touch7
In rare cases, when the device is switched on directly in defibrillator mode, cancellations of heart rhythm analysis after 30 seconds have been reported.
Recall start date: June 17, 2022
RecallHealth product recall | 2022-06-27
Merlin Patient Care System - Programmer Software
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,…
RecallHealth product recall | 2022-06-27
Intraosseous Powered Drive and Needle Kits
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.…
RecallHealth product recall | 2022-06-27
Aquac Uno H Reverse Osmosis System - Main Unit
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…
RecallHealth product recall | 2022-06-27
Tps System - Elite Burs
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…
RecallHealth product recall | 2022-06-27
Fingertip Pulse Oximeter
Voluntary recall-interim order authorisation not approved.
Recall start date: December 2, 2021
RecallHealth product recall | 2022-06-27
Digital Thermometer
Voluntary recall- interim order authorisation not approved.
Recall start date: December 2, 2021
RecallHealth product recall | 2022-06-27
Infrared Thermometer
Voluntary recall-interim order authorization not approved.
Recall start date: December 2, 2021
RecallHealth product recall | 2022-06-27
NCB Screw 5.0 L=38
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…
RecallHealth product recall | 2022-06-27
GOJO Canada Inc. recalls a lot of Purell Hand Sanitizing Wipes
The Benzalkonium Chloride assay is out of specification in the affected lot.
RecallHealth product recall | 2022-06-23
JAMP recalls vitamin D3:Out of Specification
The dissolution for vitamin D3 is out of specification in the affected lot.
RecallHealth product recall | 2022-06-22
Produits de Bien-Être Bodispa recalls sexual enhancement products due to the potential presence of undeclared prescription drug ingredients.
The products may contain undeclared ingredients which are listed on the Prescription Drug List.
RecallHealth product recall | 2022-06-21
Modular Cathcart Fracture Head
During an internal review, it was determined that the Cathcart head includes a +5mm offset, which was not specified in previous versions of the self-centering bipolar and Modular Cathcart unipolar endo heads surgical technique…
RecallHealth product recall | 2022-06-20