CLASS I Drug recall · Reported 31 Dec 2014 · FDA Enforcement Report

Ascorbic Acid 500 mg/mL Sterile Injection Multi-dose Vial recalled

Pharmacy Creations is recalling Ascorbic Acid 500 mg/mL Sterile Injection Multi-dose Vial, distributed in Florida, New Jersey, New York, Puerto Rico. The recall was initiated on 5 Sep 2014 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot #: 05082014@7, Exp 11/04/2014
Quantity recalled67 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-0305-2015
FDA event ID
69184
Recalling firm
Pharmacy Creations, Randolph, NJ
Classification
Class I
Status
Terminated
Recall initiated
5 Sep 2014
FDA classified
19 Dec 2014
Reported
31 Dec 2014
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Sterility

Timeline

5 Sep 2014Recall initiated by company
19 Dec 2014Classified by FDA+105 days
31 Dec 2014Published 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

Non-Sterility: Failing sterility results were obtained from the recalling firm's contract testing facility indicating that the products may not be sterile.

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

Ascorbic Acid 500 mg/mL Sterile Injection, 50mL Multi-dose Vial, Rx only, Pharmacy Creations, Randolph, NJ 07869 (973) 328-8756.

Where it was distributed

Directly to patients and physicians in FL, NJ, NY, and Puerto Rico

FloridaNew JerseyNew YorkPuerto Rico

Questions about this recall

Why was it recalled?

Non-Sterility: Failing sterility results were obtained from the recalling firm's contract testing facility indicating that the products may not be sterile.

Which lots are affected?

Lot #: 05082014@7, Exp 11/04/2014

Where was it sold?

Directly to patients and physicians in FL, NJ, NY, and Puerto Rico

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 69184

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