CLASS II ONGOING Drug recall · Reported 28 Oct 2020 · FDA Enforcement Report

Panagel Hand Sanitizer, 70% Alcohol recalled

Genesis Partnership is recalling Panagel Hand Sanitizer, 70% Alcohol, distributed nationwide in the US. The recall was initiated on 11 Sep 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 072120, Exp. 01/21/2022
Quantity recalled33,480 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0037-2021
FDA event ID
86427
Recalling firm
Genesis Partnership, Villa Nueva, N/A
Classification
Class II
Status
Ongoing
Recall initiated
11 Sep 2020
FDA classified
19 Oct 2020
Reported
28 Oct 2020
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

11 Sep 2020Recall initiated by company
19 Oct 2020Classified by FDA+38 days
28 Oct 2020Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

Product as listed by the FDA

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.

Where it was distributed

Nationwide in the U.S.

Nationwide

Questions about this recall

Why was it recalled?

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

Which lots are affected?

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

Where was it sold?

Nationwide in the U.S.

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

4 other products · FDA event 86427

This product is part of a recall event; the main page for the event is Genesis Hand Sanitizer Gel, Topical Solution, Non Sterile Solution recalled.

More recalls from Genesis Partnership

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