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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 90403

6 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
June 10, 2022
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Wedgewood Village Pharmacy, LLC

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

6 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 6

Bethanechol Chloride 1mg/ml, 80 ml Suspension bottles Banana/Strawberry, Qty:1, Wedgewood Village Pharmacy LLC, 405 Heron Dr. Ste 200, Swedesboro, NJ 08085

D-1181-2022
Recall number
D-1181-2022
Initiated
June 10, 2022
Classification
Class II
Status
Terminated
Quantity
1 suspension bottle

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot #: 000-03715131, Exp Date: 07/19/22

Distribution pattern

Products were distributed nationwide in the USA.

drug · product 2 of 6

Doxycycline (as Calcium) (equivalent to 50mg/5mL), 10 mg/ml, 60 ml suspension bottles, Peppermint, Qty: 1, Wedgewood Village Pharmacy LLC, 405 Heron Dr, Ste 200, Swedesboro, NJ 08085

D-1182-2022
Recall number
D-1182-2022
Initiated
June 10, 2022
Classification
Class II
Status
Terminated
Quantity
24 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot#: 000-03852523, Exp Date: 09/01/22; Lot#: 000-03766625, Exp Date:07/10/22; Lot#: 000-03780127, Exp Date: 08/6/22; Lot#: 000-03794760, Exp Date: 08/6/22; Lot#: 000-03892723, Exp Date: 09/1/22; Lot#: 000-03641022, Exp Date: 06/17/22; Lot#: 000-03693714, Exp Date: 06/28/22; Lot#: 000-03770510, Exp Date: 08/6/22; Lot#: 000-03852462, Exp Date: 09/1/22; Lot#: 000-03840601, Exp Date: 09/1/22; Lot#: 000-03706934, Exp Date: 06/28/22; Lot#: 000-03850609, Exp Date: 09/1/22; Lot#: 000-03650269, Exp Date: 06/17/22; Lot#: 000-03870004, Exp Date: 09/1/22; Lot#: 000-03693748, Exp Date: 06/28/22; Lot#: 000-03904403, Exp Date: 09/1/22; Lot#: 000-03799564, Exp Date: 08/06/22; Lot#: 000-03723022, Exp Date: 06/28/22; Lot#: 000-03872892, Exp Date: 09/01/22; Lot#: 000-03885204, Exp Date: 09/01/22; Lot#: 000-03848586, Exp Date: 09/01/22; Lot#: 000-03903599, Exp Date: 09/01/22; Lot#: 000-03812001, Exp Date: 08/06/22;

Distribution pattern

Products were distributed nationwide in the USA.

drug · product 3 of 6

Boric Acid 600 mg capsules, 14 capsules per box, Qty: 1, Wedgewood Village Pharmacy LLC, 405 Heron Drive, Ste 200, Swedesboro, NJ 08085

D-1183-2022
Recall number
D-1183-2022
Initiated
June 10, 2022
Classification
Class II
Status
Terminated
Quantity
1 box

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot#: 000-03868160, Exp Date: 09/14/22

Distribution pattern

Products were distributed nationwide in the USA.

drug · product 4 of 6

Boric Acid 600 mg per suppository, 14 Vaginal Suppositories per box, Wedgewood Village Pharmacy LLC, 405 Heron Drive, Ste 200, Swedesboro, NJ 08085

D-1184-2022
Recall number
D-1184-2022
Initiated
June 10, 2022
Classification
Class II
Status
Terminated
Quantity
14 suppositories

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot#: 000-03843532 Exp Date: 09/6/22

Distribution pattern

Products were distributed nationwide in the USA.

drug · product 5 of 6

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

D-1185-2022
Recall number
D-1185-2022
Initiated
June 10, 2022
Classification
Class II
Status
Terminated
Quantity
1 tube

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

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

Distribution pattern

Products were distributed nationwide in the USA.

drug · product 6 of 6

Estriol 1mg/gm, Vaginal Cream, 60 gm tube, Qty: 1, Wedgewood Village Pharmacy LLC, 405 Heron Drive, Ste 200, Swedesboro, NJ 08085

D-1186-2022
Recall number
D-1186-2022
Initiated
June 10, 2022
Classification
Class II
Status
Terminated
Quantity
9/18/2022

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
Lack of Processing Controls

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot#: 000-03866709 Exp Date: 09/18/22

Distribution pattern

Products were distributed nationwide in the USA.