Complete FDA and NHTSA recall records dated in 2019, 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.
Calibration failures with Std.E, Sens.E, or Dup.E error due to atypical reaction kinetics and quality control failures have occurred due to contamination of R1 reagent with R3 reagent.
Lack of an adequate sterilization validation.
Compatibility issue between the software and Microsoft updates to Windows 7, 8, and 10. The compatibility issue causes the software to be unusable which could result in a delay of reporting…
The products do not have sufficient data to support the labeled shelf life of 10 years.
Potential for failed stability antimicrobial effectiveness testing.
Mold
Stuffed Mushrooms did not declare soy as a sub ingredient of Worcestershire Sauce.
Product recalled due to a concern of possible Salmonella contamination.
Undeclared milk
The single strength apple juice is recalled because patulin was found at level greater than 50 ppb.
Product tested and found to be positive for Salmonella
White Cheddar Blend is recalled due to a potential contamination with Salmonella.
Testing revealed the presence of Listeria monocytogenes in the frozen spinach
Whole Red Raspberries are recalled due to potential contamination with Norovirus.
Testing revealed the presence of Listeria monocytogenes in the frozen spinach
Product tested and found to be positive for Salmonella
Presence of Particulate Matter; glass particulates
Lack of Assurance of Sterility: Bags have the potential to leak.
Labeling: Missing label; Product complaints reported missing bottle label.
Lack of Assurance of Sterility: Bags have the potential to leak.
BMW of North America, LLC (BMW) is recalling certain 2019 X5 xDrive50i and X7 xDrive40i vehicles. The left side wheel bolts may have been insufficiently tightened and may loosen over time.
The positive control on some tests of the lots did not appropriately react within the specified timeframe to verify the test was functioning correctly.
E-Line Cutting Electrode package 8416.0305 contains E-Line Hook Electrode 8416.09 instead of E-Line Cutting Electrode 8416.03.
The product may not have met sterility requirements . Use of a non-sterile device on a patient may expose the patient to infectious agents.
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.
