CLASS I ONGOING Drug recall · Reported 21 Jul 2021 · FDA Enforcement Report
Limar Hand Sanitizer, Isopropyl Alcohol 70%, Cont recalled
Ardil Comercial is recalling Limar Hand Sanitizer, Isopropyl Alcohol 70%, Cont. The recall was initiated on 22 Jun 2021 and the FDA has classified it as Class I.
Check your package
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-0691-2021
- FDA event ID
- 88190
- Recalling firm
- Ardil Comercial, Santo Domingo Este
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 22 Jun 2021
- FDA classified
- 20 Jul 2021
- Reported
- 21 Jul 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Packaging Defects
- Drug class
- Hand Sanitizer
Timeline
| 22 Jun 2021 | Recall initiated by company | |
| 20 Jul 2021 | Classified by FDA | +28 days |
| 21 Jul 2021 | Published in enforcement report | +1 day |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
Limar Hand Sanitizer, Isopropyl Alcohol 70%, Cont. 4 oz bottles, Manufactured in Dominican Republic: by Ardil Comercial S.R.L., Santo Domingo, Dominican Republic UPC 7 487040 301587
Where it was distributed
Product was distributed to one client in NYC who further distributed the product.
Questions about this recall
Why was it recalled?
Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.
Which lots are affected?
Batch Number # 079932-4611-05-J, exp. date May 2022
Where was it sold?
Product was distributed to one client in NYC who further distributed the product.
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 I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
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.