Overview of recall records associated with Mckesson Medical-Surgical Inc. Corporate Office, including dates, categories and classifications where available.
Classification mix: Class II: 109, Class III: 23.
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between…
CGMP Deviations: products were stored outside the drug label specifications.
CGMP Deviations: products were stored outside the drug label specifications.
CGMP Deviations: products were stored outside the drug label specifications.
CGMP Deviations: products were stored outside the drug label specifications.
CGMP Deviations: products were stored outside the drug label specifications.
CGMP Deviations: products were stored outside the drug label specifications.
CGMP Deviations: products were stored outside the drug label specifications.
CGMP Deviations: products were stored outside the drug label specifications.
cGMP deviations: Temperature abuse
cGMP deviations: Temperature abuse
Two unsuitable 3mL syringes with conventional needles for vaccine administration included in some Moderna 140 Ancillary Convenience Kits.
This page summarizes recall records in which the official source identifies Mckesson Medical-Surgical Inc. Corporate Office 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.
