Recall events
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Event 80963
Event summary
Timeline bucket August 31, 2018
Product types Drug
Classifications Class II
Statuses Terminated
Recalling firm wording Beaumont Bio-med, Inc.
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
8 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 8
Skin Irritation & Itch Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7002-7
D-1192-2018
Recall number D-1192-2018
Initiated August 31, 2018
Classification Class II
Status Terminated
Quantity 192 bottles
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
Microbial contamination
reason.microbial_contamination · v1.0.0
microbial contamination
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Code information Lot: 091515C, Exp 09/2018; 050118S, Exp 05/2021
Distribution pattern 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[10356]
FDA event record
· Exact recall-number query on openFDA
drug · product 2 of 8
Sinus Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7013-7
D-1193-2018
Recall number D-1193-2018
Initiated August 31, 2018
Classification Class II
Status Terminated
Quantity 90 bottles
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
Microbial contamination
reason.microbial_contamination · v1.0.0
microbial contamination
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Code information Lot: 100316A, Exp 10/2019
Distribution pattern 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[9977]
FDA event record
· Exact recall-number query on openFDA
drug · product 3 of 8
Sore Throat & Laryngitis Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7014-7
D-1194-2018
Recall number D-1194-2018
Initiated August 31, 2018
Classification Class II
Status Terminated
Quantity 420 bottles
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
Microbial contamination
reason.microbial_contamination · v1.0.0
microbial contamination
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Code information Lot: 100316G, Exp 10/2019; 050118R, Exp 05/2021
Distribution pattern 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[9885]
FDA event record
· Exact recall-number query on openFDA
drug · product 4 of 8
Diarrhea Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7022-7
D-1195-2018
Recall number D-1195-2018
Initiated August 31, 2018
Classification Class II
Status Terminated
Quantity 160 bottles
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
Microbial contamination
reason.microbial_contamination · v1.0.0
microbial contamination
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Code information Lot: 090915A, Exp 09/2018
Distribution pattern 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[8082]
FDA event record
· Exact recall-number query on openFDA
drug · product 5 of 8
Muscle & Joint Pain Relief Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7041-7
D-1196-2018
Recall number D-1196-2018
Initiated August 31, 2018
Classification Class II
Status Terminated
Quantity 109 bottles
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
Microbial contamination
reason.microbial_contamination · v1.0.0
microbial contamination
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Code information Lot: 012916F, Exp 01/2019
Distribution pattern 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[10014]
FDA event record
· Exact recall-number query on openFDA
drug · product 6 of 8
Allergy & Hay Fever Relief Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7011-7
D-1197-2018
Recall number D-1197-2018
Initiated August 31, 2018
Classification Class II
Status Terminated
Quantity 124 bottles
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
Microbial contamination
reason.microbial_contamination · v1.0.0
microbial contamination
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Code information Lot: 050216X, Exp 05/2019
Distribution pattern 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[9971]
FDA event record
· Exact recall-number query on openFDA
drug · product 7 of 8
Colds & Flu Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7012-7
D-1198-2018
Recall number D-1198-2018
Initiated August 31, 2018
Classification Class II
Status Terminated
Quantity 314 bottles
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
Microbial contamination
reason.microbial_contamination · v1.0.0
microbial contamination
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Code information Lot: 042816C, Exp 04/2019; 112317K, Exp 11/2020
Distribution pattern 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[9877]
FDA event record
· Exact recall-number query on openFDA
drug · product 8 of 8
Arthritis Pain Relief Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7042-7
D-1199-2018
Recall number D-1199-2018
Initiated August 31, 2018
Classification Class II
Status Terminated
Quantity 140 bottles
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
Microbial contamination
reason.microbial_contamination · v1.0.0
microbial contamination
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Code information Lot: 012916E, Exp 01/2019
Distribution pattern 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[9983]
FDA event record
· Exact recall-number query on openFDA
