Exact FDA event identifier

Event 92453

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

Event summary

Timeline bucket: June 05, 2023
Product types: Drug
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Homeocare Laboratories, 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

11 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 11

Kanjo Homeopathic Pain Relief Cream With Arnica, NET WT 2 oz (56.70G), Manufactured For: Acutens, Inc., Sheridan, WY NDC 80551-201-02

D-0880-2023

Recall number: D-0880-2023
Initiated: June 05, 2023
Classification: Class II
Status: Terminated
Recalling firm: Homeocare Laboratories, Inc.
Quantity: 921 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

cGMP deviations

Code information

Lot # 2446, exp. date Mar-24

Distribution pattern

Product was distributed USA nationwide.

drug · product 2 of 11

Arnica 7 Cream, net wt 2 oz (56.7g), Manufactured for: Brazmedics, LLC, New York, NY 10021 UPC 8 60208 00181 6

D-0881-2023

Recall number: D-0881-2023
Initiated: June 05, 2023
Classification: Class II
Status: Terminated
Recalling firm: Homeocare Laboratories, Inc.
Quantity: 2,376 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

cGMP deviations

Code information

Lot # 2446, exp. Mar-24

Distribution pattern

Product was distributed USA nationwide.

drug · product 3 of 11

Bebelyn Colic Drops Homeopathic Remedy, 0.5 FL Oz (15 mL) bottles, distributed by Pharmadel LLC Georgetown, DE NDC 55758-036-01

D-0882-2023

Recall number: D-0882-2023
Initiated: June 05, 2023
Classification: Class II
Status: Terminated
Recalling firm: Homeocare Laboratories, Inc.
Quantity: 5,956 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

cGMP deviations

Code information

Lot # 2414, exp. date Sep-24

Distribution pattern

Product was distributed USA nationwide.

drug · product 4 of 11

Babelyn Diarrhea Drops Homeopathic Remedy, 0.5 fl. oz. (15 mL) bottles, Distributed by Pharmadel LLC, Georgetown, DE NDC 55758-035-01

D-0883-2023

Recall number: D-0883-2023
Initiated: June 05, 2023
Classification: Class II
Status: Terminated
Recalling firm: Homeocare Laboratories, Inc.
Quantity: 5957 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

cGMP deviations

Code information

Lot # 2413, exp. date Sep-24

Distribution pattern

Product was distributed USA nationwide.

drug · product 5 of 11

DoloEar Earache Drops, 0.50 fl. oz. bottles, Distributed by Pharmadel LLC, Georgetown, DE NDC 55758-001-15

D-0884-2023

Recall number: D-0884-2023
Initiated: June 05, 2023
Classification: Class II
Status: Terminated
Recalling firm: Homeocare Laboratories, Inc.
Quantity: 12,850 tottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

cGMP deviations

Code information

Lot # 2423, exp. date Nov-24; 2445, exp. date Apr-25

Distribution pattern

Product was distributed USA nationwide.

drug · product 6 of 11

SnoreStop Naso Spray Bulk, liquid, Distributed by Green Pharma, NDC 61152-199-99

D-0885-2023

Recall number: D-0885-2023
Initiated: June 05, 2023
Classification: Class II
Status: Terminated
Recalling firm: Homeocare Laboratories, Inc.
Quantity: 200 liters/55 gallon drum

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

cGMP deviations

Code information

Lot # 2436, exp. date: unknown

Distribution pattern

Product was distributed USA nationwide.

drug · product 7 of 11

StellaLife VEGA Oral Care Rinse, 16 fl oz (473 ml) bottles, Peppermint, Distributed by: StellaLife, Inc., Aventura, FL NDC 69685-103-16

D-0886-2023

Recall number: D-0886-2023
Initiated: June 05, 2023
Classification: Class II
Status: Terminated
Recalling firm: Homeocare Laboratories, Inc.
Quantity: 130,762/16 oz. tottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

cGMP deviations

Code information

Lot # 2357B,2333, exp. date Sep-2; 2367C, 2367D, exp. date Nov-23; 2367E, 2367F, exp. date Jan-24; 2395A, 2406, exp. date Feb-2; 2395B, exp. date Mar-24; 2395C, exp. date Apr-24

Distribution pattern

Product was distributed USA nationwide.

drug · product 8 of 11

StellaLife VEGA Oral Care Rinse, 16 fl oz (473 ml) bottles, Coconut, Distributed by: StellaLife, Aventura, FL NDC 69685-113-16

D-0887-2023

Recall number: D-0887-2023
Initiated: June 05, 2023
Classification: Class II
Status: Terminated
Recalling firm: Homeocare Laboratories, Inc.
Quantity: 16,587 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

cGMP deviations

Code information

Lot # 2396, exp. date Apr-24

Distribution pattern

Product was distributed USA nationwide.

drug · product 9 of 11

StellaLife VEGA Oral Care Spray, 1 fl oz (30 ml) bottles, Distributed by: StellaLife, Inc., Aventura, FL NDC 69685-101-02

D-0888-2023

Recall number: D-0888-2023
Initiated: June 05, 2023
Classification: Class II
Status: Terminated
Recalling firm: Homeocare Laboratories, Inc.
Quantity: 40,034/1 fl. oz tubes

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

cGMP deviations

Code information

Lot # 2335, exp. date Sep-23; 2364, exp. date Nov-23; 2408, exp. date Feb-24

Distribution pattern

Product was distributed USA nationwide.

drug · product 10 of 11

StellaLife VEGA Oral Care Gel, 1 fl oz (30 ml) tubes, Distributed by: StellaLife, Inc., Aventura, FL NDC 69685-102-02

D-0889-2023

Recall number: D-0889-2023
Initiated: June 05, 2023
Classification: Class II
Status: Terminated
Recalling firm: Homeocare Laboratories, Inc.
Quantity: 38,105/1 fl. oz. tubes

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

cGMP deviations

Code information

Lot #2334, exp. date Sep-23; 2363, exp. date Nov-23; 2365, exp. date Jan-24

Distribution pattern

Product was distributed USA nationwide.

drug · product 11 of 11

StellaLife VEGA Oral Care Gel, 1 fl oz (30 ml) tubes, Peppermint, Distributed by: StellaLife, Inc., Aventura, FL NDC 69685-112-01

D-0890-2023

Recall number: D-0890-2023
Initiated: June 05, 2023
Classification: Class II
Status: Terminated
Recalling firm: Homeocare Laboratories, Inc.
Quantity: 33,109/1 fl. oz. tubes

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

cGMP deviations

Code information

Lot #2407, exp. date Feb-24; 2409A, exp. date Apr-24; 2409B, exp. date May-24

Distribution pattern

Product was distributed USA nationwide.