Complete FDA and NHTSA recall records dated in 2020, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
Notified by customer of reports of illness after consuming tuna steaks, found high levels of histamines.
Products are being recalled due to Listeria monocytogenes contamination.
Products are being recalled due to Listeria monocytogenes contamination.
Product is recalled due to consumer complaints for bloating of package, off flavors (sourness, tart), and textural issues (grittiness, lumpiness).
Undeclared Walnut Allergen. Maple Walnut Probiotic granola was packaged in Chocolate Sea Salt probiotic granola bags.
The product contains undeclared sulfites.
CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
Failed Tablet/Capsule Specifications: Complaints related to crumbling of tablets when popped out of the blister pack.
Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
Toyota Motor Engineering & Manufacturing (Toyota) recalled certain 2018-2019 4Runner, Highlander, Camry, Land Cruiser, Sequoia, Sienna, Tacoma and Tundra, and Lexus RC 300, RC 350, GS 350,…
Potential power issues with the Accu-Chek Guide Blood Glucose Monitoring System.
There is a potential hardware error for the iMRX System with a generator A100. A tolerance issue in the power supply of the generator control above a specific value may cause generator A100…
Due to a manufacturing issue affecting particular O-arm" O2 Imaging Systems, Medtronic has determined that the gantry tractor motor drive belt may loosen over an extended number of uses at…
Potential power issues with the Accu-Chek Guide Blood Glucose Monitoring System.
Potential power issues with the Accu-Chek Guide Blood Glucose Monitoring System.
A component failure may lead to treatment interruption or incorrect source positioning.
An amendment to the IFU and Service Manual is being issued to prescribe the replacement of the angulation chain after 8 years of service of the of the unit. After testing, it was found that…
Potential power issues with the Accu-Chek Guide Blood Glucose Monitoring System.
The products are labeled as Class II lasers. However, the level of laser radiation emitted by the distributed products may exceed the limit (1 mW) established for Class II lasers. These…
Invia Foam Dressing Kit with FitPad could have holes in the sterile packaging.
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.
