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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 86427

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

Open FDA event record

Event summary

Timeline bucket
September 11, 2020
Product types
Drug
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Genesis Partnership Company SA

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

5 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 5

Panagel Hand Sanitizer, 70% Alcohol,16 Fl. Oz. (472 mL) bottle, Made in Guatemala, Distributed by Central Med Distribution, 6100 Hollywood Blvd, Hollywood FL 33024, NDC 78384-001-04, UPC 378384000016.

D-0037-2021
Recall number
D-0037-2021
Initiated
September 11, 2020
Classification
Class II
Status
Ongoing
Quantity
33,480 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviations: hand sanitizers were recalled because they were manufactured in the same facility as another hand sanitizer product with sub-potent ethanol levels.

Code information

Lot #: 072120, Exp. 01/21/2022

Distribution pattern

Nationwide in the U.S.

drug · product 2 of 5

Genesis Hand Sanitizer Gel, Topical Solution, Non Sterile Solution, 240 mL (8 FL OZ.) bottle, Manufactured by Genesis Partnership Company S.A., Guatemala, NDC 74484-002-02, UPC 7401037205773.

D-0038-2021
Recall number
D-0038-2021
Initiated
September 11, 2020
Classification
Class II
Status
Ongoing
Quantity
15,000 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviations: hand sanitizers were recalled because they were manufactured in the same facility as another hand sanitizer product with sub-potent ethanol levels.

Code information

Lot #: 37009, Exp. 02/10/2021

Distribution pattern

Nationwide in the U.S.

drug · product 3 of 5

Genesis Hand Sanitizer Gel, Topical Solution, Non Sterile Solution, 1 gallon (3785 mL) bottle, Manufactured by Genesis Partnership Company S.A., Guatemala, NDC 74484-002-04, UPC 7401037203427.

D-0039-2021
Recall number
D-0039-2021
Initiated
September 11, 2020
Classification
Class II
Status
Ongoing
Quantity
5,040 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviations: hand sanitizers were recalled because they were manufactured in the same facility as another hand sanitizer product with sub-potent ethanol levels.

Code information

Lot #: 37009, Exp. 02/10/2021

Distribution pattern

Nationwide in the U.S.

drug · product 4 of 5

Killz Germz Hand Sanitizer, Alcohol Gel, 450 mL (15 fl oz.) bottle, Manufactured by Genesis Partnership Company S.A., Guatemala, For: Killz Germz, LLC., 1912 R street NW, Washington DC, 20009, NDC 74625-003-04, UPC 7401037203250.

D-0040-2021
Recall number
D-0040-2021
Initiated
September 11, 2020
Classification
Class II
Status
Ongoing
Quantity
5,320 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing revealed ethanol levels as low as 62% while labelled claim is 70%.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing revealed ethanol levels as low as 62% while labelled claim is 70%.

Code information

Lot #s: 36748, 36818, 36697, Exp. 10/15/21 and 11/8/21

Distribution pattern

Nationwide in the U.S.

drug · product 5 of 5

Killz Germz Hand Sanitizer, Alcohol Gel, 1 Gallon (128 fl. oz.) bottle, Manufactured by Genesis Partnership Company S.A., Guatemala, For: Killz Germz, LLC., 1912 R street NW, Washington DC 20009, NDC 74625-003-05, UPC 7401037203427.

D-0041-2021
Recall number
D-0041-2021
Initiated
September 11, 2020
Classification
Class II
Status
Ongoing
Quantity
8600 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing revealed ethanol levels as low as 62% while labelled claim is 70%.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing revealed ethanol levels as low as 62% while labelled claim is 70%.

Code information

Lot #s: 36748, 36818, 36697, Exp. 10/15/21 and 11/8/21

Distribution pattern

Nationwide in the U.S.