Recall events
/
Event 81218
Event summary
Timeline bucket October 09, 2018
Product types Drug
Classifications Class II
Statuses Terminated
Recalling firm wording Sprayology
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
22 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 22
Rejuvenation Plus, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879 NDC 61096-0035-1
D-0105-2019
Recall number D-0105-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 1,558 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 All lots within expiry
Distribution pattern 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[10355]
FDA event record
· Exact recall-number query on openFDA
drug · product 2 of 22
Man Power, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0025-1 and Tester NDC 61096-1025-1
D-0106-2019
Recall number D-0106-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 830 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 All lots within expiry
Distribution pattern 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[10476]
FDA event record
· Exact recall-number query on openFDA
drug · product 3 of 22
Brain Power,Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0033-1
D-0107-2019
Recall number D-0107-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 2,054 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 All lots within expiry
Distribution pattern 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[10075]
FDA event record
· Exact recall-number query on openFDA
drug · product 4 of 22
Woman Power, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879 NDC 61096-0034-1 and Tester NDC 61096-1034-1
D-0108-2019
Recall number D-0108-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 1,284 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 All lots within expiry
Distribution pattern 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[10339]
FDA event record
· Exact recall-number query on openFDA
drug · product 5 of 22
MenoPower, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0014-1 and Tester NDC 61096-1014
D-0109-2019
Recall number D-0109-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 2,301 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 All lots within expiry
Distribution pattern 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[10332]
FDA event record
· Exact recall-number query on openFDA
drug · product 6 of 22
Bone Builder, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0012-1 and Tester NDC 61096-1012-1
D-0110-2019
Recall number D-0110-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 731 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 All lots within expiry
Distribution pattern 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[10498]
FDA event record
· Exact recall-number query on openFDA
drug · product 7 of 22
AllergEase, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0003-1
D-0111-2019
Recall number D-0111-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 4,153 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 All lots within expiry
Distribution pattern 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[10405]
FDA event record
· Exact recall-number query on openFDA
drug · product 8 of 22
Cold + Flu Relief, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0002-1
D-0112-2019
Recall number D-0112-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 2,565 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 All lots within expiry
Distribution pattern 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[8107]
FDA event record
· Exact recall-number query on openFDA
drug · product 9 of 22
DigestivEase, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879.NDC 61096-0005-1
D-0113-2019
Recall number D-0113-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 1,465 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 All lots within expiry
Distribution pattern 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[10048]
FDA event record
· Exact recall-number query on openFDA
drug · product 10 of 22
SleepEase, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879.NDC 61096-0001-1 and Tester NDC 6196-1001-1
D-0114-2019
Recall number D-0114-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 5,393 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 All lots within expiry
Distribution pattern 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[10082]
FDA event record
· Exact recall-number query on openFDA
drug · product 11 of 22
TravelEase, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879NDC 61096-0007-1. and Tester NDC 61096-1007-1
D-0115-2019
Recall number D-0115-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 1,307 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 All lots within expiry
Distribution pattern 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[10064]
FDA event record
· Exact recall-number query on openFDA
drug · product 12 of 22
Party Relief, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0030-1 and Tester NDC 61096-1030-1
D-0116-2019
Recall number D-0116-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 2,956 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 All lots within expiry
Distribution pattern 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[10055]
FDA event record
· Exact recall-number query on openFDA
drug · product 13 of 22
Arnica Power, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879.NDC 61096-0032-1
D-0117-2019
Recall number D-0117-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 3,531 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 All lots within expiry
Distribution pattern 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[8126]
FDA event record
· Exact recall-number query on openFDA
drug · product 14 of 22
Snore Soother, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0024-1
D-0118-2019
Recall number D-0118-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 1,055 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 All lots within expiry
Distribution pattern 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[10117]
FDA event record
· Exact recall-number query on openFDA
drug · product 15 of 22
Stress Relief, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0006-1 and Tester NDC 61096-1006-1
D-0119-2019
Recall number D-0119-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 3,896 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 All lots within expiry
Distribution pattern 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[10457]
FDA event record
· Exact recall-number query on openFDA
drug · product 16 of 22
PMS Support, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0031-1
D-0120-2019
Recall number D-0120-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 647 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 All lots within expiry
Distribution pattern 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[10465]
FDA event record
· Exact recall-number query on openFDA
drug · product 17 of 22
Life Detoxer Homeopathic Oral Spray 1.38 fl. oz. (41 mL). Manufactured by Sprayology Gaithersburg, MD 20879NDC 61096-0023-1 and Tester NDC 61096-1023-1
D-0121-2019
Recall number D-0121-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 1,473 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 All lots within expiry
Distribution pattern 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[10107]
FDA event record
· Exact recall-number query on openFDA
drug · product 18 of 22
ImmunoBooster, Homeopathic Oral Spray 1.38 fl. oz. (41 mL). Manufactured by Sprayology Gaithersburg, MD 20879. NDC 61096-0038-1
D-0122-2019
Recall number D-0122-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 2,837 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 All lots within expiry
Distribution pattern 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[10204]
FDA event record
· Exact recall-number query on openFDA
drug · product 19 of 22
Body Skin Tonic, Homeopathic Oral Spray 1.38 fl. oz. (41 mL). Manufactured by Sprayology Gaithersburg, MD 20879. NDC 61096-0017-1
D-0123-2019
Recall number D-0123-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 857 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 All lots within expiry
Distribution pattern 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[8096]
FDA event record
· Exact recall-number query on openFDA
drug · product 20 of 22
Acne Tonic Homeopathic Oral Spray 1.38 fl. oz. (41 mL). Manufactured by Sprayology Gaithersburg, MD 20879. NDC 61096-0027-1
D-0124-2019
Recall number D-0124-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 919 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 All lots within expiry
Distribution pattern 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[10358]
FDA event record
· Exact recall-number query on openFDA
drug · product 21 of 22
Body Balance, Homeopathic Oral Spray 1.38 fl. oz (41 mL). Manufactured by Sprayology Gaithersburg, MD 20879. NDC 61096-0039-1
D-0125-2019
Recall number D-0125-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 2,595 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 All lots within expiry
Distribution pattern 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[10461]
FDA event record
· Exact recall-number query on openFDA
drug · product 22 of 22
Diet Power, Homeopathic Oral Spray 1.38 fl. oz. (41 mL). Manufactured by Sprayology Gaithersburg, MD 20879. NDC 61096-0004-1
D-0126-2019
Recall number D-0126-2019
Initiated October 09, 2018
Classification Class II
Status Terminated
Quantity 3634 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 All lots within expiry
Distribution pattern 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[10326]
FDA event record
· Exact recall-number query on openFDA
