Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Ongoing Initiated Mar 7, 2022 (5 years ago)

Methionine/Inositol/Choline B12 25mg/50mg/50mg/1mg/mL

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Assurance of Sterility

Cause type: Sterility / contamination

A product that must be sterile could not be assured sterile, or was contaminated. A top reason for injectables, eye drops and IV products - loss of sterility assurance can lead to serious infections. All sterility / contamination recalls.

What was recalled

Methionine/Inositol/Choline B12 25mg/50mg/50mg/1mg/mL, a)10 mL-vial, b) 30 mL-vial, Room Temperature, Tailor Made Compounding

Drug: Methionine

Recalling firm
TMC Acquisition LLC dba Tailor Made Compounding
Origin
KY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1214-2022 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall.

Other Methionine recalls

See all
Class II · Moderate risk

LX Bioboost Plus

Lack of Assurance of Sterility

Ongoing Sterility / contamination Thrive Health and Wellness, LLC, dba Thrive Health Solutions (Colorado) D-0477-2025
Class II · Moderate risk

Micc

Lack of assurance of sterility.

Completed Sterility / contamination Olympia Compounding Pharmacy dba Olympia Pharmacy NDC 73198-0052-10 D-0937-2022

Other recalls by TMC Acquisition LLC dba Tailor Made Compounding

All 2022 recalls