BayCare Integrated Service Center, LLC /dba Iohexol (300 mg Iodine/mL), 2.4 g Iodine/8 ml recall — FDA D-0086-2023
Labeling: Label Error on Declared Strength: syringes mislabeled as 300 mg iodine/mL contained product 350 mg iodine/mL
Overview of recall records associated with BayCare Integrated Service Center, LLC /dba BayCare Central Pharmacy, including dates, categories and classifications where available.
Classification mix: Class I: 1.
Labeling: Label Error on Declared Strength: syringes mislabeled as 300 mg iodine/mL contained product 350 mg iodine/mL
This page summarizes recall records in which the official source identifies BayCare Integrated Service Center, LLC /dba BayCare Central Pharmacy 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.