FDA recall record

The Apothecary Shoppe S-methylcobalamin 25 mg/mL (PF) Injection recall — FDA D-1292-2015

Lack of Assurance of Sterility: Due to lack of documentation of proper environmental monitoring during the time in which the medication was produced.

Class IIclassification
D-1292-2015official record ID
Aug 12, 2015report date

Recall record at a glance

Official recordD-1292-2015
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmThe Apothecary Shoppe LLC
Report dateAug 12, 2015
Recall initiation dateJun 26, 2015
Quantity25.3 mL
LocationTulsa, OK, United States

Official product description

S-methylcobalamin 25 mg/mL (PF) Injection, Rx Only, 10 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13861-1701-19

Why the product was recalled

Lack of Assurance of Sterility: Due to lack of documentation of proper environmental monitoring during the time in which the medication was produced.

Distribution information

Oklahoma

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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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