CLASS II Drug recall · Reported 13 Jul 2022 · FDA Enforcement Report
Boric Acid 600 mg per suppository recalled by Wedgewood Village Pharmacy
Wedgewood Village Pharmacy is recalling Boric Acid 600 mg per suppository, 14 Vaginal Suppositories per, Wedgewood Village, 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
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-1184-2022
- 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
- Processing Deviation
Timeline
| 10 Jun 2022 | Recall initiated by company | |
| 7 Jul 2022 | Classified by FDA | +27 days |
| 13 Jul 2022 | Published 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
The USDA issues these when meat or poultry was produced without proper inspection, or when a step such as cooking or pasteurisation did not meet requirements.
Product as listed by the FDA
Boric Acid 600 mg per suppository, 14 Vaginal Suppositories per box, Wedgewood Village Pharmacy LLC, 405 Heron Drive, Ste 200, Swedesboro, NJ 08085
Where it was distributed
Products were distributed nationwide in the USA.
Questions about this recall
Why was it recalled?
Lack of Processing Controls: Insanitary conditions observed during recent FDA Inspection
Which lots are affected?
Lot#: 000-03843532 Exp Date: 09/6/22
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 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
5 other products · FDA event 90403This product is part of a recall event; the main page for the event is Bethanechol Chloride 1mg/ml Suspension bottles recalled.
More recalls from Wedgewood Village Pharmacy
All 6| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Estriol 1mg/gm, Vaginal Cream, 30 gm tube, Qty recalled | Wedgewood Village Pharmacy | Processing Deviation | Nationwide |
| Drug | CLASS II | Boric Acid per, Qty: 1, Wedgewood Village Pharmacy LLC recalled | Wedgewood Village Pharmacy | Processing Deviation | Nationwide |
| Drug | CLASS II | Doxycycline (as Calcium) (equivalent to 50mg recalled | Wedgewood Village Pharmacy | Processing Deviation | Nationwide |
| Drug | CLASS II | Estriol 1mg/gm, Vaginal Cream, 60 gm tube, Qty recalled | Wedgewood Village Pharmacy | Processing Deviation | Nationwide |
| Drug | CLASS II | Bethanechol Chloride 1mg/ml Suspension bottles recalled | Wedgewood Village Pharmacy | Processing Deviation | Nationwide |