CLASS II Drug recall · Reported 5 Jun 2013 · FDA Enforcement Report

PHMB Opth Soln 02% Opthalmic Soln, 30 day recalled

Nora Apothecary and Alternative Therapies is recalling PHMB Opth Soln 02% Opthalmic Soln, 30 day, distributed nationwide in the US. The recall was initiated on 22 Apr 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll products within their expiration date including those dated 90 days prior to April 19, 2013 (Jan. 2013 to April 19, 2013).
Quantity recalled2

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-474-2013
FDA event ID
65019
Recalling firm
Nora Apothecary and Alternative Therapies, Indianapolis, IN
Classification
Class II
Status
Terminated
Recall initiated
22 Apr 2013
FDA classified
29 May 2013
Reported
5 Jun 2013
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Sterility

Timeline

22 Apr 2013Recall initiated by company
29 May 2013Classified by FDA+37 days
5 Jun 2013Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

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

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Is PHMB Opth Soln 02% Opthalmic Soln, 30 day recalled?

Yes. Nora Apothecary and Alternative Therapies recalled PHMB Opth Soln 02% Opthalmic Soln, 30 day on 22 Apr 2013. The recall is Class II and its status is Terminated. Recall number D-474-2013.

Why was it recalled?

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

Which lots are affected?

All products within their expiration date including those dated 90 days prior to April 19, 2013 (Jan. 2013 to April 19, 2013).

Where was it sold?

Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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