CLASS II Drug recall · Reported 19 Jun 2019 · FDA Enforcement Report

Bacteriostatic Water for Injection vials, Pharm D recalled

Pharm D Solutions is recalling Bacteriostatic Water for Injection vials, Pharm D, distributed nationwide in the US. The recall was initiated on 23 May 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 11292018:75 Exp. 05/28/2019; 01022019:70 Exp. 07/01/2019; 02042019:04 Exp. 08/03/2019; 03042019:94 Exp. 08/31/2019
Quantity recalled716 vials

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-1322-2019
FDA event ID
82941
Recalling firm
Pharm D Solutions, Houston, TX
Classification
Class II
Status
Terminated
Recall initiated
23 May 2019
FDA classified
7 Jun 2019
Reported
19 Jun 2019
Type
FDA Mandated
Customers notified by
Press Release
Reason category
Sterility

Timeline

23 May 2019Recall initiated by company
7 Jun 2019Classified by FDA+15 days
19 Jun 2019Published in enforcement report+12 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 Sterility Assurance.

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

Bacteriostatic Water for Injection, 10 mL vials, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846

Where it was distributed

Nationwide within the United States

Nationwide

Questions about this recall

Is Bacteriostatic Water for Injection vials, Pharm D recalled?

Yes. Pharm D Solutions recalled Bacteriostatic Water for Injection vials, Pharm D on 23 May 2019. The recall is Class II and its status is Terminated. Recall number D-1322-2019.

Why was it recalled?

Lack of Sterility Assurance.

Which lots are affected?

Lot #: 11292018:75 Exp. 05/28/2019; 01022019:70 Exp. 07/01/2019; 02042019:04 Exp. 08/03/2019; 03042019:94 Exp. 08/31/2019

Where was it sold?

Nationwide within the United States

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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