Severity
Critical
CriticalClass IOngoing
FDA Drug recall · Reported July 21, 2021
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
Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.
Ardil Comercial S.r.l. recalled Limar Hand Sanitizer, Isopropyl Alcohol 70%, Cont. 4 oz bottles, Manufactured in Dominica… - a critical-severity action.
Limar Hand Sanitizer, Isopropyl Alcohol 70%, Cont. 4 oz bottles, Manufactured in Dominica… was recalled by Ardil Comercial S.r.l. in July 21, 2021. Reason: Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.. Check the official notice for the remedy. Verify recall #D-0691-2021 with the FDA Drug before acting.
The recall
Ardil Comercial S.r.l. issued this critical-severity FDA Drug recall-Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles..
- Critical
- severity level
- Class I
- classification
- July 21, 2021
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0691-2021 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0691-2021) was formally reported on July 21, 2021, with the manufacturer initiating the action on June 22, 2021. It is classified under Critical severity (Class I), with a current status of Ongoing. Ardil Comercial S.r.l. is listed as the recalling firm, operating out of Santo Domingo Este. Federal records list the affected scope as 1,260 bottles.
The documented reason for this recall is: Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles. Distribution data in the federal record shows the product reached: Product was distributed to one client in NYC who further distributed the product.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
1,260 bottles
Related Recalls
6
5 from same agency
Product description
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
Reason for recall
Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Ongoing |
| Recall number | D-0691-2021 |
| Date reported | July 21, 2021 |
| Date initiated | June 22, 2021 |
| Recalling firm | Ardil Comercial S.r.l. |
| Firm location | Santo Domingo Este |
| Affected scope | 1,260 bottles |
| Distribution | Product was distributed to one client in NYC who further distributed the product. |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0691-2021) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Ardil Comercial S.r.l.. Units affected: 1,260 bottles.
Why was this product recalled? ▼
Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 21, 2021. Severity: Critical. Recall number: D-0691-2021.
Where was the recalled product distributed? ▼
Distribution: Product was distributed to one client in NYC who further distributed the product..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0691-2021) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with PRED MILD, prednisolone acetate ophthalmic suspension, USP,… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported July 21, 2021. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.