FDA recall record

American Health Packaging Cyanocobalamin Injection, USP, 1000 mcg per mL, For Intramuscular recall — FDA D-0790-2022

Subpotent Drug: Out of specification for assay.

Class IIIclassification
D-0790-2022official record ID
May 4, 2022report date

Recall record at a glance

Official recordD-0790-2022
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmAmerican Health Packaging
Report dateMay 4, 2022
Recall initiation dateApr 12, 2022
Quantity97,975 vials
LocationColumbus, OH, United States

Official product description

Cyanocobalamin Injection, USP, 1000 mcg per mL, For Intramuscular or Subcutaneous Use Only, 25 x 1 mL Vials, Rx only, Manufactured by: Eugia Pharma Specialties Limited, Hyderabad India for BluePoint Laboratories. NDC for Carton: 68001-509-60; NDC for vial: 68001-509-59

Why the product was recalled

Subpotent Drug: Out of specification for assay.

Distribution information

Alabama

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

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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