Zyprexa Intramuscular, Olanzapine for Injection, 10 MG per Single Use Vial, Rx only, Marketed by: Lilly USA, LLC, Indianapolis, IN 46285, NDC# 0002-7597-01
Reported: August 18, 2021 Initiated: June 29, 2021 #D-0720-2021
Product Description
Zyprexa Intramuscular, Olanzapine for Injection, 10 MG per Single Use Vial, Rx only, Marketed by: Lilly USA, LLC, Indianapolis, IN 46285, NDC# 0002-7597-01
Reason for Recall
cGMP deviations: Atypical appearance, decrease in size and change in color of the lyophilized cake of drug product.
Details
- Recalling Firm
- Eli Lilly & Company
- Units Affected
- 36,540 vials
- Distribution
- OH, MS, IN
- Location
- Indianapolis, IN
Frequently Asked Questions
What product was recalled? ▼
Zyprexa Intramuscular, Olanzapine for Injection, 10 MG per Single Use Vial, Rx only, Marketed by: Lilly USA, LLC, Indianapolis, IN 46285, NDC# 0002-7597-01. Recalled by Eli Lilly & Company. Units affected: 36,540 vials.
Why was this product recalled? ▼
cGMP deviations: Atypical appearance, decrease in size and change in color of the lyophilized cake of drug product.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 18, 2021. Severity: Moderate. Recall number: D-0720-2021.
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