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Displaying 1 - 3 of 3 items.
Mani Diamond Tomita-Saw
The manufacturer, a third-party supplier (Mani, Inc.), discontinued production of the Mani™ Diamond Tomita-Saw™ product and subsequently terminated the medical device license for this device.
Recall start date: Nov 24, 2021
RecallHealth product recall | 2022-03-28
Architect "I" System - Stat Myoglobin Assay
The purpose of this recall is to inform the customer of a product recall for architect stat myoglobin calibrators, ln 2k43-01, lot number 166000. They have identified that this calibrator lot did not meet acceptance criteria during ongoing stability…
RecallHealth product recall | 2022-03-14
Restore Wound Cleanser
The product license is on hold/suspended due to the missing MDSAP certification from the supplier Biomed. Since there is no MDSAP certification the products are not meeting the regulatory requirements of the act or MDR for Health Canada (Medical Devices…
RecallHealth product recall | 2022-03-14