Key Takeaway

Chlorhexidine Opth Soln 0.02%, 10 ml Opthalmic Soln, 30 day expiration, by Nora Apothecary and Alternative Therapies, Inc. was recalled on April 22, 2013. The hazard: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.

FDA Drug Class II Terminated

Chlorhexidine Opth Soln 0.02%, 10 ml Opthalmic Soln, 30 day expiration,

Recalled: April 22, 2013 ~1 units affected D-472-2013

Description

Chlorhexidine Opth Soln 0.02%, 10 ml Opthalmic Soln, 30 day expiration,

Hazard / Reason

Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.

Class II: Product that may cause temporary or medically reversible health consequences.

Class II indicates the product may cause temporary or medically reversible health effects. The probability of serious harm is considered remote.

Products Affected

Chlorhexidine Opth Soln 0.02%, 10 ml Opthalmic Soln, 30 day expiration,

Drugs

Company Information

Nora Apothecary and Alternative Therapies, Inc.

Indianapolis, IN, United States

View all 43 recalls by Nora Apothecary and Alternative Therapies, Inc. →

Distribution

Nationwide

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Frequently Asked Questions

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Check the status badge at the top of this page. "Ongoing" means the recall is still active and you should follow the remedy instructions. "Completed" or "Terminated" means the recall process has concluded, though the safety issue remains relevant for any unrepaired products.

How do I check if my product is affected?

Compare the model number, lot code, serial number, or date range listed in the recall notice with the information on your product's label or packaging. For vehicles, check your VIN at NHTSA.gov/Recalls.

What remedy is available for this recall?

Check the remedy section above or contact the manufacturer directly for current remedy options.

Where can I find the original recall notice?

This recall was issued by FDA Drug. Visit the agency's official website for the original notice.

Data sourced from FDA Drug Enforcement. Recall information may not reflect the most current status. RecallDex is not affiliated with any US government agency. Contact the manufacturer or relevant agency for the latest information.