Medline E-Z Lubricating Jelly recall — FDA Z-0984-2017
Product was not sterilized. Product was shipped to distribution centers instead of the sterilization facility due to an operations error by a 3rd party shipping company.
Overview of recall records associated with MEDLINE IND, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Product was not sterilized. Product was shipped to distribution centers instead of the sterilization facility due to an operations error by a 3rd party shipping company.
This page summarizes recall records in which the official source identifies MEDLINE IND 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.