Recall events
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Event 90403
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
Device root-cause evidence is not applicable to this event.
No grouped product has the official product type device; this is not an unavailable-enrichment finding.
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.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[12628]
FDA event record
· Exact recall-number query on openFDA
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.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[13128]
FDA event record
· Exact recall-number query on openFDA
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.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[13126]
FDA event record
· Exact recall-number query on openFDA
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.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[12448]
FDA event record
· Exact recall-number query on openFDA
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.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[12449]
FDA event record
· Exact recall-number query on openFDA
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.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[12630]
FDA event record
· Exact recall-number query on openFDA