FDA recall record

Phytonadione Injectable Emulsion USP, 10 mg/mL, 25x 1 mL single dose ampules per carton recall — FDA D-0007-2023

Failed Stability Specifications: Out of specification results reported at 12-month stability testing for aluminum content.

Class IIIclassification
D-0007-2023official record ID
Oct 12, 2022report date

Recall record at a glance

Official recordD-0007-2023
CategoryDrug Recalls
ClassificationClass III
FDA record statusCompleted
Recalling firmDr. Reddy's Laboratories, Inc.
Report dateOct 12, 2022
Recall initiation dateSep 14, 2022
Quantity2,838 ampules
LocationPrinceton, NJ, United States

Official product description

Phytonadione Injectable Emulsion USP, 10 mg/mL, 25x 1 mL single dose ampules per carton, Rx only, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, NDC 43598-405-16

Why the product was recalled

Failed Stability Specifications: Out of specification results reported at 12-month stability testing for aluminum content.

Distribution information

USA nationwide

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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