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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Wedgewood Village Pharmacy Medications Recalled for Insanitary Conditions

Agency Publication Date: July 7, 2022
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Summary

Wedgewood Village Pharmacy, LLC is recalling approximately 50 units of various prescription medications, including Bethanechol Chloride, Doxycycline, Boric Acid, and Estriol. This voluntary recall was initiated after an FDA inspection revealed a lack of processing controls and insanitary conditions at the manufacturing facility. While no injuries or illnesses have been reported to date, these conditions could lead to drug contamination that compromises patient safety. Affected products were distributed nationwide throughout the United States between June and September 2022.

Risk

The medications were produced under insanitary conditions and without proper processing controls, which may result in product contamination. Use of contaminated drugs poses a risk of infection or other serious adverse health reactions, particularly for patients with weakened immune systems or those using vaginal creams and suppositories.

What You Should Do

  1. This recall affects various medications prepared by Wedgewood Village Pharmacy LLC, including Bethanechol Chloride, Doxycycline, Boric Acid capsules and suppositories, and Estriol vaginal cream.
  2. Check your medication packaging for the following identifying details: Bethanechol Chloride 1mg/ml (Lot 000-03715131, Exp 07/19/22), Boric Acid 600 mg capsules (Lot 000-03868160, Exp 09/14/22), Boric Acid 600 mg suppositories (Lot 000-03843532, Exp 09/6/22), Estriol 1mg/gm 30g tube (Lot 000-03807142, Exp 08/27/22), and Estriol 1mg/gm 60g tube (Lot 000-03866709, Exp 09/18/22).
  3. For Doxycycline 10 mg/ml suspension (60 ml peppermint flavor), check the lot number printed on your bottle. See the Affected Products section below for the full list of affected codes.
  4. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Wedgewood Village Pharmacy LLC for further instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Bethanechol Chloride 1mg/ml (80 ml)
Variants: Suspension, Banana/Strawberry
Lot Numbers:
000-03715131 (Exp 07/19/22)

Recall #: D-1181-2022

Product: Doxycycline (as Calcium) 10 mg/ml (60 ml)
Variants: Suspension, Peppermint
Lot Numbers:
000-03852523 (Exp 09/01/22)
000-03766625 (Exp 07/10/22)
000-03780127 (Exp 08/6/22)
000-03794760 (Exp 08/6/22)
000-03892723 (Exp 09/1/22)
000-03641022 (Exp 06/17/22)
000-03693714 (Exp 06/28/22)
000-03770510 (Exp 08/6/22)
000-03852462 (Exp 09/1/22)
000-03840601 (Exp 09/1/22)
000-03706934 (Exp 06/28/22)
000-03850609 (Exp 09/1/22)
000-03650269 (Exp 06/17/22)
000-03870004 (Exp 09/1/22)
000-03693748 (Exp 06/28/22)
000-03904403 (Exp 09/1/22)
000-03799564 (Exp 08/06/22)
000-03723022 (Exp 06/28/22)
000-03872892 (Exp 09/01/22)
000-03885204 (Exp 09/01/22)
000-03848586 (Exp 09/01/22)
000-03903599 (Exp 09/01/22)
000-03812001 (Exp 08/06/22)

Recall #: D-1182-2022

Product: Boric Acid 600 mg capsules (14 capsules per box)
Variants: Capsules
Lot Numbers:
000-03868160 (Exp 09/14/22)

Recall #: D-1183-2022

Product: Boric Acid 600 mg per suppository (14 per box)
Variants: Vaginal Suppositories
Lot Numbers:
000-03843532 (Exp 09/6/22)

Recall #: D-1184-2022

Product: Estriol 1mg/gm Vaginal Cream (30 gm tube)
Variants: Cream, 1mg/gm
Lot Numbers:
000-03807142 (Exp 08/27/22)

Recall #: D-1185-2022

Product: Estriol 1mg/gm Vaginal Cream (60 gm tube)
Variants: Cream, 1mg/gm
Lot Numbers:
000-03866709 (Exp 09/18/22)

Recall #: D-1186-2022

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 90403
Status: Resolved
Manufacturer: Wedgewood Village Pharmacy, LLC
Sold By: Wedgewood Village Pharmacy LLC
Manufactured In: United States
Units Affected: 6 products (1 suspension bottle; 24 bottles; 1 box; 14 suppositories; 1 tube; 9/18/2022)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.