McConnell ’ s Fine Ice Creams Recalls Select 16oz. Packages Due To Possible Health Risk
Santa Barbara, CA - Out of an abundance of caution, McConnell ’ s Fine Ice Creams is undertaking a voluntary recall of selected, 16 oz. (pint size) packages of ice cream produced by a contract manufacturer because they have the potential to be contaminated with Listeria monocytogenes. (Source: FDA Food Safety)
Source: FDA Food Safety - November 4, 2016 Category: Food Science Source Type: alerts

Kellogg Company Voluntarily Recalls Limited Number of Kellogg ’ s ® Eggo ® Nutri-Grain ® Whole Wheat Waffles Due to Potential Health Risk
Kellogg Company is voluntarily recalling approximately 10,000 cases of Kellogg ’ s ® Eggo ® Nutri-Grain ® Whole Wheat Waffles because they have the potential to be contaminated with Listeria monocytogenes. No other Eggo products are impacted by this recall. (Source: FDA Food Safety)
Source: FDA Food Safety - September 20, 2016 Category: Food Science Source Type: alerts

Expanded Recall Period of Certain Sunflower Kernel Products Due to Possible Contamination By Listeria Monocytogenes
TORONTO - As a precaution, SunOpta expanded its voluntary recall of a limited number of sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women. (Source: FDA Food Safety)
Source: FDA Food Safety - May 19, 2016 Category: Food Science Source Type: alerts

Beckman Coulter Inc. - MicroScan Pos Breakpoint Combo Panel Type 23 - Class 2 Recall
MicroScan Pos Breakpoint Combo Panel Type 23, Part No. B1017-206 MicroScan Pos (Positive) panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of rapidly growing aerobic and facultative gram-positive cocci, some fastidious aerobic gram-positive cocci and Listeria monocytogenes. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 31, 2015 Category: Medical Equipment Source Type: alerts

Beckman Coulter Inc. - MicroScan Pos Combo Panel Type 33 - Class 2 Recall
MicroScan Pos Combo Panel Type 33, Part No. B1017-211 MicroScan Pos (Positive) panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of rapidly growing aerobic and facultative gram-positive cocci, some fastidious aerobic gram-positive cocci and Listeria monocytogenes. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 31, 2015 Category: Medical Equipment Source Type: alerts

Beckman Coulter Inc. - MicroScan Pos Combo Panel Type 21 - Class 2 Recall
MicroScan Pos Combo Panel Type 21, Part No. B1017-201 MicroScan Pos (Positive) panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of rapidly growing aerobic and facultative gram-positive cocci, some fastidious aerobic gram-positive cocci and Listeria monocytogenes. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 31, 2015 Category: Medical Equipment Source Type: alerts

Beckman Coulter Inc. - MicroScan Pos Breakpoint Combo Panel Type 20 - Class 2 Recall
MicroScan Pos Breakpoint Combo Panel Type 20, Part No. B1017-202 MicroScan Pos (Positive) panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of rapidly growing aerobic and facultative gram-positive cocci, some fastidious aerobic gram-positive cocci and Listeria monocytogenes. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 31, 2015 Category: Medical Equipment Source Type: alerts

Beckman Coulter Inc. - MicroScan Pos Combo Panel Type 34 - Class 2 Recall
MicroScan Pos Combo Panel Type 34, Part No. B1017-214 MicroScan Pos (Positive) panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of rapidly growing aerobic and facultative gram-positive cocci, some fastidious aerobic gram-positive cocci and Listeria monocytogenes. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 31, 2015 Category: Medical Equipment Source Type: alerts

BACTERIA PLUS (Adenosinum Triphosphoricum Dinatrum, Malic Acid, Natrum Oxalaceticum, Oroticum Acidum, Riboflavinum, Apiolum, Cinnamic Acid, Streptococcus Viridans, Pneumococcinum, Colibacillinum Cum Natrum Muriaticum, Echinacea (Angustiolia), Helicobacter Pylori, Mycoplasma Pneumoniae, Proteus (Mirabilis), Proteus (Vulgaris), Pseudomonas Aeruginosa, Yersinia Enterocolitica, Streptococcus Agalactiae, Legionella Pneumophila, Enterococcus Faecalis, Streptococcus Mutans, Listeria Monocytogenes, Dysentery Bacillus) Liquid [Deseret Biologicals, Inc.]
Updated Date: Feb 19, 2015 EST (Source: DailyMed Drug Label Updates for the last seven days (since May 20, 2007 EST))
Source: DailyMed Drug Label Updates for the last seven days (since May 20, 2007 EST) - February 19, 2015 Category: Drugs & Pharmacology Source Type: alerts

Nanosphere, Inc. - Class 2 Recall
The Verigene Gram-Positive Blood Culture Nucleic Acid Test (BC-UP) performed using the sample-to-result Verigene System is a qualitative, multiplexed in vitro diagnostic test for the simultaneous detection and identification of potentially pathogenic gram-positive bacteria which may cause bloodstream infection (BSI). BC-UP is performed directly on blood culture bottles identified as positive by a continuous monitoring blood culture system and which contain gram-positive bacteria. BC-UP detects and identifies the following bacterial genera and species: Staphylococcus spp., Staphylococcus aureus, Staphylococcus epidermidis, ...
Source: Medical Device Recalls - September 24, 2014 Category: Medical Equipment Source Type: alerts

BioFire Diagnostics, Inc. - FilmArray Blood Culture Identification (BCID) Panel - Class 2 Recall
FirmArray Blood Culture Identification (BCID) Panel, Model 2.0 The FilmArray Blood Culture Identification (BCID) Panel is a qualitative multiplexed nucleic acid-based in vitro diagnostic test designed to test positive blood cultures to quickly identify the organism that is growing in the blood culture. The following gram-positive bacteria, gram-negative bacteria, and yeast are identified using the FilmArray BCID Panel: Enterococci, Listeria monocytogenes, commonly encountered Staphylococci (including specific differentiation of Staphylococcus aureus), commonly encountered Streptococci (with specific differentiation of S...
Source: Medical Device Recalls - June 21, 2014 Category: Medical Equipment Source Type: alerts

BioMerieux SA - API Listeria (REF 10300) - Class 2 Recall
API Listeria (REF 10300). ZYM B reagent is used and included inside of API NH (REF 10400) and API Listeria (10300). All of the API s are standardized systems combining several biochemical tests that enable group or species identification of most microorganisms. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 19, 2014 Category: Medical Equipment Source Type: alerts

BioMerieux SA - API NIH (REF 10400) - Class 2 Recall
API NIH (REF 10400). ZYM B reagent is used and included inside of API NH (REF 10400) and API Listeria (10300). All of the API's are standardized systems combining several biochemical tests that enable group or species identification of most microorganisms. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 19, 2014 Category: Medical Equipment Source Type: alerts

Biomerieux France Chemin De L'Or - API Listeria (REF 10300)) - Class 2 Recall
API Listeria (REF 10300) API Listeria is a standardized system for the identification of Listeria which uses miniaturized tests, as well as a database. The ZYM B reagent is including in API Listeria kit and it is used as an additional reagent for revealing the result of DIM miniaturized biochemical test included in the API Listeria strips. ZYM B reagent is added in the DIM test before reading miniaturized biochemical test including in the API Listeria strips. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 28, 2014 Category: Medical Equipment Source Type: alerts