Complete FDA and NHTSA recall records dated in November 2018.
These records include useful source details for the selected month.
The apple juice concentrates contain high levels of inorganic arsenic. The firm is recalling lots that were distributed for use other than fermentation (i.e. alcohol or vinegar).
Positive result for Salmonella received while investigating to determine supplier of direct customer's positive findings also for Salmonella
Frozen non-ready to eat Alaskan Salmon Bites, Kroger brand, are recalled due to potential contamination with Listeria monocytogenes or Salmonella in vegetables ingredient.
Hot & Sour Broth product contains Tamari which contains sub ingredient soybeans but finished label does not declare soy.
The firm was notified by their supplier that the vegetables used in the product were possibly contaminated with Listeria monocytogenes and Salmonella.
Cinnamon Chip Sourdough Village Baker brand was recalled because the label does not declare sub ingredients milk powder and soy lecithin.
During FDA inspection it was found that soy oil was not declared on package label
Angel Food Cake Bar was recalled due to undeclared milk and soy. The actual product inside container is corn breads and it was mislabeled as Angel Food Cake Bar.
Routine quality testing identified elevated levels of lead above applicable 2232 levels, which may pose potential health risks to a portion of the population.
Complaints of insects in product
Labeling: Incorrect or Missing Lot and/or Expiration Date; vial indicates a 1 year expiration date instead of a 6 month expiration date
Microbial Contamination of Non-Sterile Product
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
CGMP Deviations: Product was released to market prior to microbiological testing.
Labeling: Incorrect Instructions; Instructions included for use with the Veridate dispenser contained instructions for the Dialpak dispenser.
Failed pH Specifications: Upward shift in the pH of the solution within the shelf life of the impacted lots.
Lack of Assurance of Sterility; bags have the potential to leak
Labeling: Incorrect Instructions; Instructions included for use with the Veridate dispenser contained instructions for the Dialpak dispenser.
CGMP Deviations: Product was released to market prior to microbiological testing.
Volvo Car USA LLC (Volvo) is recalling certain 2017-2019 Volvo XC90, S90, V60, V60 Cross Country, V90, XC40, XC60, and V90 Cross Country vehicles. The software installed in the Vehicle…
Honda (American Honda Motor Co.) is recalling certain model year 2018 and 2019 Honda Odyssey vehicles. The latch assemblies for the power sliding doors may stick and not properly latch to…
Defect with the calibration button for lot 1808M. Level 1 and Level 2 Quality Control (QC) values will generate results of HIGH (>65 ¿g/dL). Results for patient testing with this lot will…
The product is labeled with an incorrect expiration date.
The press fit connection of the Angular Sleeve and pin of the U-Joint and Click Lock did not meet specification. A dimensional discrepancy of the bore hole of the Angular Sleeve may cause a…
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
