Class I · High riskTerminated Initiated Dec 4, 2017 (9 years ago)
Pantoprazole Sodium for Injection, 40 mg per vial, single dose vial, Rx only…
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Presence of Particulate Matter: One vial from a lot of Pantoprazole Sodium for Injection (40 mg) contained a piece of glass
What was recalled
Pantoprazole Sodium for Injection, 40 mg per vial, single dose vial, Rx only, Manufactured in India for: AuroMedics Pharma LLC, 6 Wheeling ROad, Dayton, NJ 08810. NDC 55150-202-00
Recalling firm
AuroMedics Pharma LLC
NDC code
55150-202-00
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0340-2018
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Reason CGMP Deviations; The impacted product and lot number was inadvertently placed into saleable inventory, which does not comply with approved procedures.