Wedgewood Village Pharmacy recalls 14-count boric acid vaginal suppositories due to insanitary conditions found during FDA inspection. Consumers should check lot numbers and expiration dates.
Lack of Processing Controls: Insanitary conditions observed during recent FDA Inspection
Wedgewood Village Pharmacy is recalling 14-vaginal suppository packs of boric acid 600 mg per suppository because of insanitary conditions observed during an FDA inspection. This recall affects products with lot number 000-03843532 that expired September 6, 2022.
The FDA found insanitary conditions during a recent inspection, which could lead to contamination of the suppositories. This poses a risk of infection or other health issues if the product is used without proper hygiene.
People who purchased the recalled boric acid vaginal suppositories from Wedgewood Village Pharmacy in Swedesboro, NJ. Those using the product for medical purposes are most at risk due to potential contamination.
Check for the lot number 000-03843532 on the packaging. The product expires September 6, 2022, and was sold by Wedgewood Village Pharmacy in Swedesboro, NJ.
Look for the lot number 000-03843532 and expiration date of September 6, 2022 on the packaging.
The FDA found insanitary conditions during an inspection, so the product may be contaminated. Do not use until the recall is resolved.
Check for the lot number 000-03843532 and expiration date of September 6, 2022 on the packaging.
The recall does not specify a remedy, so contact Wedgewood Village Pharmacy for guidance.
We’ve drafted a message you can send Wedgewood Village Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-1184-2022 — Wedgewood Village Pharmacy Wedgewood Village Pharmacy Hello, I own a Wedgewood Village Pharmacy that is covered by recall D-1184-2022 from Wedgewood Village Pharmacy. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
