OraSure Technologies, Inc. - Personelle OTC Skin Tag Remover - Class 3 Recall
Personelle OTC Skin Tag Remover, Canada Catalog Number: 1001-0314 - Product Usage: indicated for over-the-counter a cryosurgical system for the treatment of skin tags. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 24, 2020 Category: Medical Devices Source Type: alerts
LABORIE MEDICAL TECHNOLOGIES, CANADA ULC - Pump Tube Set for MMS Libra and Solar Systems - Class 2 Recall
Pump Tube Set for MMS Libra and Solar Systems - Product Usage: Intended for use during water perfusion urodynamic procedures to study the function of the bladder and urethra during filling and voiding, by monitoring pressure and pressure changes. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 8, 2020 Category: Medical Devices Source Type: alerts
CHANGE HEALTHCARE CANADA COMPANY - McKesson Cardiology ECG Management, Change Healthcare Cardiology ECG Management - Class 2 Recall
McKesson Cardiology ECG Management, Change Healthcare Cardiology ECG Management (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 9, 2020 Category: Medical Devices Source Type: alerts
Qiagen Sciences LLC - AmniSure ROM Test - Class 2 Recall
AmniSure ROM Test, Material Nos. FMRT-1-25-US (US Distribution, 25 tests/box), FMRT-1-10-US (US Distribution, 10 tests/box), FMRT-1-25-CA (Canadian Distribution; 25 tests/box) (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 2, 2020 Category: Medical Devices Source Type: alerts
Abbott GmBH & Co. KG - Alinity c Carbon Dioxide Reagent Kit - Class 2 Recall
Alinity c Carbon Dioxide Reagent Kit, Produced for Abbott by Sekisui Diagnostics P.E.I. Inc. Prince Edward Island Canada (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 27, 2019 Category: Medical Devices Source Type: alerts
Becton Dickinson & Company - BD - Class 2 Recall
BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575 (Canada only) (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 21, 2019 Category: Medical Devices Source Type: alerts
Mann Packing Co., Inc. Voluntarily Recalls Vegetable Products Sold in the United States and Canada Due to Potential Health Risks
The voluntary recall is a response to a notification by the Food and Drug Administration and the Canadian Food Inspection Agency of a potential contamination with Listeria monocytogenes. (Source: FDA Food Safety)
Source: FDA Food Safety - November 4, 2019 Category: Food Science Authors: FDA Source Type: alerts
VOLUMEN (Barium Sulfate) Suspension [E-Z-EM Canada Inc]
Updated Date: Wed, 23 Oct 2019 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 23, 2019 Category: Drugs & Pharmacology Source Type: alerts
NITROGEN (Nitrogen) Gas [Messer Canada LTD]
Updated Date: Fri, 18 Oct 2019 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 18, 2019 Category: Drugs & Pharmacology Source Type: alerts
OXYGEN Gas [Messer Canada LTD]
Updated Date: Fri, 18 Oct 2019 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 18, 2019 Category: Drugs & Pharmacology Source Type: alerts
CU PAIN AWAY PAIN RELIEF (Menthol) Cream [Canadian Unique Health Ltd.]
Updated Date: Tue, 15 Oct 2019 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 15, 2019 Category: Drugs & Pharmacology Source Type: alerts
Abbott Laboratories Recalls Calcilo XD ® Infant Formula
Out of an abundance of caution, Abbott has voluntarily recalled a single lot of Calcilo XD ® powder cans (13.2oz / 375g) with lot number 79696K80 in the United States and Canada due to an inconsistency in aroma and color in a small number of cans from this specific batch. (Source: FDA Food Safety)
Source: FDA Food Safety - October 9, 2019 Category: Food Science Authors: FDA Source Type: alerts
BAT (Botulism Antitoxin Heptavalent) Liquid [Emergent BIoSolutions Canada Inc.]
Updated Date: Mon, 07 Oct 2019 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 7, 2019 Category: Drugs & Pharmacology Source Type: alerts
The J. M. Smucker Company Issues Voluntary Recall of Specific Lots of Robin Hood ® All Purpose Flour Distributed and Sold in the U.S. Only
Out of an abundance of caution, The J. M. Smucker Company today announced a voluntary recall of specific lots of Robin Hood ® All Purpose Flour distributed and sold in the U.S. due to possible E. coli contamination. This recall does not impact any Robin Hood® items sold in Canada. (Source: FDA Food Safety)
Source: FDA Food Safety - October 4, 2019 Category: Food Science Authors: FDA Source Type: alerts
The Metrix Company - SECURE EVA DUAL CHAMBER CONTAINER - Class 2 Recall
SECURE EVA - DUAL CHAMBER CONTAINER with Manifold, 1500mL, REF 66616 (Canadian distribution) - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 2, 2019 Category: Medical Devices Source Type: alerts
