FDA recall record

Innovative Intrathecal Solutions, Inc. dba MIC-8 recall — FDA D-1096-2020

Lack of Assurance of Sterility

Class IIclassification
D-1096-2020official record ID
Apr 15, 2020report date

Recall record at a glance

Official recordD-1096-2020
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmInnovative Intrathecal Solutions, Inc. dba Innovative Compounding Pharmacy
Report dateApr 15, 2020
Recall initiation dateMar 26, 2020
QuantityN/A
LocationMurrieta, CA, United States

Official product description

MIC-8 (Methionine 15mg /Inositol 50 mg/Choline 100 mg/B-12 6mcg/ml) , 10 mL, Injectable, Rx only, INNOVATIVE COMPOUNDING PHARMACY, 41536 EASTMAN DRIVE SUITE A MURRIETA , CA 92562 951-304-9530

Why the product was recalled

Lack of Assurance of Sterility

Distribution information

Patient Distribution list includes addresses in the following states: CA, ME, TX

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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