Class II · Moderate risk Ongoing
Vancomycin HCL
Reason Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Vancomycin 25 mg/mL Opthalmic Solution
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.
What was recalled
Vancomycin 25 mg/mL Opthalmic Solution, packaged in a) 10 mL bottle and b) 15 mL bottle, Rx only, Liberty Drug Compound Center, 195 Main St., PO Box 267, Chatham, NJ 07928.
- Recalling firm
- Liberty Drug & Surgical
- Origin
- NJ, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1387-2015
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 Vancomycin recalls
See all
Class II · Moderate risk Ongoing
Vancomycin HCI
Reason Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Class II · Moderate risk Ongoing
Vancomycin HCI
Reason Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Class II · Moderate risk Ongoing
vancomycin HCl
Reason Lack of Assurance of Sterility
Class II · Moderate risk Ongoing
vancomycin HCl
Reason Lack of Assurance of Sterility
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