Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 86327

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

Open FDA event record

Event summary

Timeline bucket
August 25, 2020
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Asiaticon, SA de CV

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

2 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 2

V-Klean Hand Sanitizer Gel Alcohol 70% packaged as a)8.5 fl oz (250 ml), UPC 7 16053 70499 3; b) 16.9 fl oz (500 ml), UPC 7 16053 70499 3; c) 33.8 fl. oz. (1000 ml) bottles: 716053704993; Manufactured by: Asiaticon S.A. de C.V. Conkar 62, Jardines del Ajusco. Tlalpan Cuidad de Mexico. 14200 ;

D-0116-2021
Recall number
D-0116-2021
Initiated
August 25, 2020
Classification
Class II
Status
Terminated
Recalling firm
Asiaticon, SA de CV
Quantity
111,500 units

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
Lack of CGMPs

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of CGMPs:

Code information

All lots.

Distribution pattern

Distributed in Texas

drug · product 2 of 2

Protz real protection Antibacterial Hand Sanitizer, Ethyl Alcohol 70%, 13.5 FL OZ (400 mL), Distributed by: Safety-Med Products, Inc. Burlington, WI 53105 Made in Mexico by Asiaticon S.A. de C.V. Conkal No. 62, Mexico, Ciudad de Mexico 14200, Mexico NDC: 75192-600-02 UPC 7 503019 005002

D-0117-2021
Recall number
D-0117-2021
Initiated
August 25, 2020
Classification
Class II
Status
Terminated
Recalling firm
Asiaticon, SA de CV
Quantity
111,500 units

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
Lack of CGMPs

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of CGMPs:

Code information

All lots.

Distribution pattern

Distributed in Texas

Field note

Send feedback

We'll only use this to respond to your feedback.