Gasco Isopropyl Alcohol 70%, Net Contents: 16 Oz. (474 mL). Manufactured by: Gasco Industrial Corp., PO Box 1360 Gurabo
Summary
The FDA issued a Class II for Gasco Isopropyl Alcohol 70%, Net Contents: 16 Oz. (474 mL). Manufactured by: Gas by Gasco Industrial Corp.. Reason: Subpotent drug.
Details
Source
Drug Recall
External ID
D-0665-2026
Action Date
2026-07-15
Status
Ongoing
Category
drug
Product Description
Gasco Isopropyl Alcohol 70%, Net Contents: 16 Oz. (474 mL). Manufactured by: Gasco Industrial Corp., PO Box 1360 Gurabo PR 00778 Made in USA UPC 7 87302 13044 3
Lot/Code Info: Lot 250306B3, within expiry
Quantity Affected: N/A
Reason for Recall
Subpotent drug
Distribution
Nationwide within the US
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-29
Company
Gurabo, PR
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 44 drug recalls issued in the same week, part of 93 drug-related FDA actions this month.
Gasco Industrial Corp. has 6 FDA actions in our database, including 6 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Gasco Industrial Corp.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Gasco Industrial Corp. have FDA actions?
Gasco Industrial Corp. has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0665-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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