Bayer Healthcare Bronkaid Dual Action Formula, Ephedrine Sulfate 25 mg/Bronchodilator recall — FDA D-177-2013
Labeling: Label lacks warning or Rx legend; Certain information was inadvertently excluded from the product carton label.
Overview of recall records associated with Bayer Healthcare, LLC, including dates, categories and classifications where available.
Classification mix: Class III: 3.
Labeling: Label lacks warning or Rx legend; Certain information was inadvertently excluded from the product carton label.
Labeling: Label Mix-up: This recall was initiated after identifying that the label statement on the blister strip regarding the maximum number of capsules/caplets that should be taken…
Labeling: Label Mix-up: This recall was initiated after identifying that the label statement on the blister strip regarding the maximum number of capsules/caplets that should be taken…
This page summarizes recall records in which the official source identifies Bayer Healthcare, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.