CLASS II Drug recall · Reported 13 Jul 2022 · FDA Enforcement Report

Estriol 1mg/gm, Vaginal Cream, 30 gm tube, Qty recalled

Wedgewood Village Pharmacy is recalling Estriol 1mg/gm, Vaginal Cream, 30 gm tube, Qty: 1, Wedgewood Village Pharmacy LLC, 405, distributed nationwide in the US. The recall was initiated on 10 Jun 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot#: 000-03807142 Exp Date: 08/27/22
Quantity recalled1 tube

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-1185-2022
FDA event ID
90403
Recalling firm
Wedgewood Village Pharmacy, Swedesboro, NJ
Classification
Class II
Status
Terminated
Recall initiated
10 Jun 2022
FDA classified
7 Jul 2022
Reported
13 Jul 2022
Type
Voluntary: Firm initiated
Customers notified by
N/A
Reason category
Foreign Material

Timeline

10 Jun 2022Recall initiated by company
7 Jul 2022Classified by FDA+27 days
13 Jul 2022Published in enforcement report+6 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 Processing Controls: Insanitary conditions observed during recent FDA Inspection

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Estriol 1mg/gm, Vaginal Cream, 30 gm tube, Qty: 1, Wedgewood Village Pharmacy LLC, 405 Heron Drive, Ste 200, Swedesboro, NJ 08085

Where it was distributed

Products were distributed nationwide in the USA.

Nationwide

Questions about this recall

Is Estriol 1mg/gm, Vaginal Cream, 30 gm tube, Qty: 1, Wedgewood Village Pharmacy LLC, 405 recalled?

Yes. Wedgewood Village Pharmacy recalled Estriol 1mg/gm, Vaginal Cream, 30 gm tube, Qty: 1, Wedgewood Village Pharmacy LLC, 405 on 10 Jun 2022. The recall is Class II and its status is Terminated. Recall number D-1185-2022.

Why was it recalled?

Lack of Processing Controls: Insanitary conditions observed during recent FDA Inspection

Which lots are affected?

Lot#: 000-03807142 Exp Date: 08/27/22

Where was it sold?

Products were distributed nationwide in the USA.

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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