Class II · Moderate risk Terminated
B-Complex
Reason Presence of Particulate Matter.
Riboflavin 0.1% Ophthalmic Solution Syringe
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Assurance of Sterility
What was recalled
RIBOFLAVIN 0.1% OPHTHALMIC SOLUTION SYRINGE, 2 ML per syringe. RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0923-02
- Recalling firm
- RXQ Compounding LLC
- Origin
- OH, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1701-2019
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Riboflavin recalls
See all
Class II · Moderate risk Terminated
Thiamine/Ribofla/Niacinami/Dexpanth/Pyridox/Hydroxycobal…
Reason Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Class II · Moderate risk Terminated
Thiamine Hydrochloride 3000 mg/30 mL
Reason Presence of Particulate Matter: Presence of foreign substances were reported in vials at the pharmacy.
Class II · Moderate risk Terminated
Thiamine Hydrochloride 200 mg/2mL
Reason Presence of Particulate Matter: Presence of foreign substances were reported in vials at the pharmacy.
Class II · Moderate risk Terminated
B-Complex + Chromic Chloride
Reason Lack of Assurance of Sterility
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