Gasco Isopropyl Alcohol 70% recall — Gasco Industrial Corp. (Class II)

Gasco Industrial Corp. is recorded by the U.S. Food and Drug Administration (FDA) as recalling Gasco Isopropyl Alcohol 70% — a Class II recall, initiated 2026-05-29 and posted to the FDA enforcement report on 2026-07-15, under recall number D-0665-2026. Status Ongoing, with no termination date on the record. The reason the FDA record carries is, verbatim: “Subpotent drug”. From the product description, the strengths given are 70%, 474 mL and 1360 G. The record carries UPC 787302130443 rather than an NDC. Distribution is recorded as “Nationwide within the US” — Nationwide (US), with the recalling firm on record in PR, United States. The FDA files it under event ID 99138 together with 5 other recall numbers, all listed and linked below. Within that event this is the strength 70% · 474 mL · 1360 G and product named Gasco Isopropyl Alcohol 70% configuration; the sibling records differ on strength and product named and match on everything else the source states. Values are reproduced from the linked openFDA report; regulatory information, not medical advice.

Regulatory snapshot

Recall number D-0665-2026
FDA event ID 99138 (6 recall numbers)
Classification Class II (intermediate regulatory tier)
Status Ongoing
Recalling firm Gasco Industrial Corp.
Recall initiated 2026-05-29
Reported by FDA 2026-07-15
Report lag 47 days from initiation to report
Distribution Nationwide within the US — Nationwide (US)
Firm location on record PR, United States
Product description (source) 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

Reason reported by FDA

Subpotent drug

2 words from the enforcement report field reason_for_recall, reproduced without edit — the firm's own wording, not an assessment.

Product identifiers in this record

6 identifying values matched by exact pattern in the 29-word product description above; each is a literal substring of it.

Product named Gasco Isopropyl Alcohol 70%
Strength 70% · 474 mL · 1360 G
UPC 787302130443
Stated origin USA
Manufactured by Gasco Industrial Corp., PO Box 1360 Gurabo PR 00778 Made in USA UPC 7 87302 13044 3

Which configuration this record is

6 recall numbers share event 99138. They differ on strength and product named and agree on everything else the source states, so those are the values to check a package against.

Attribute This record (D-0665-2026) D-0666-2026D-0667-2026D-0668-2026D-0669-2026D-0670-2026
Strength 70% · 474 mL · 1360 G 70% · 3.78 L70% · 946 mL70% · 1 g · 3.78 l70% · 474 mL70% · 946 mL
Product named Gasco Isopropyl Alcohol 70% Gasco Isopropyl Alcohol 70%Gasco Isopropyl Alcohol 70%Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%

Shared across all 6 records under this event: fda tier Class II; recalling firm Gasco Industrial Corp.; reason text Subpotent drug; initiated 2026-05-29; reported 2026-07-15.

Event context: 6 recall numbers under event 99138

One enforcement action, 6 recall numbers: the FDA filed 5 further configurations of this action under event 99138. Each keeps its own recall number and dates.

Recall recordRecall numberFDA tierStrength / formReported
Gasco Isopropyl Alcohol 70%D-0666-2026Class II70%2026-07-15
Gasco Isopropyl Alcohol 70%D-0667-2026Class II70%2026-07-15
Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%D-0668-2026Class II70%2026-07-15
Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%D-0669-2026Class II70%2026-07-15
Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%D-0670-2026Class II70%2026-07-15

Reported in the same month (2026-07)

111 enforcement reports carry a report date in 2026-07; these 8 are the Class II ones nearest this record.

Recall recordRecall numberRecalling firmFDA tierReported
Methohexital Sodium for Injection, 500 mgD-0662-2026Onesource Specialty Pharma LtdClass II2026-07-15
Medline Remedy Specialized Silicone Cream (Hydraguard-D ), 59 mLD-0663-2026Biomed Laboratories, Llc.Class II2026-07-15
Methohexital Sodium, 100 mg/10 mLD-0664-2026Quva Pharma, Inc.Class II2026-07-15
Pemetrexed for Injection 100mg/VialD-0671-2026Reliance Life Sciences Private LtdClass II2026-07-15
Pemetrexed for Injection 500mg/VialD-0672-2026Reliance Life Sciences Private LtdClass II2026-07-15
Bortezomib for Injection 3.5mg/VialD-0673-2026Reliance Life Sciences Private LtdClass II2026-07-15
Azacitidine for Injection 100mg/VialD-0674-2026Reliance Life Sciences Private LtdClass II2026-07-15
Clomiphene Citrate USP Active Pharmaceutical Ingredient (CAS : 50-41-9), 1 KGD-0691-2026Shimoga ChemicalsClass II2026-07-15

Nearest Class II recalls by date

213 of 250 indexed records share the Class II tier; the 3 nearest to 2026-07-15 by report date are listed here.

Recall recordRecall numberRecalling firmStrength / formReported
BD ChloraPrep Hi-Lite Orange, 2%D-0643-2026Carefusion 213, LLC2% · Solution2026-07-08
BD PurPrep, 8.3%D-0644-2026Carefusion 213, LLC8.3% · Solution2026-07-08
BD ChloraPrep Clear, 2%D-0645-2026Carefusion 213, LLC2% · Solution2026-07-08

Reading this record

Class II is the FDA's own severity tier for the recall action — 213 of the 250 indexed records carry it — and it describes the agency's assessment of the action, not a risk statement about any individual. A search on event 99138 returns all 6 of these recall numbers; a search on D-0665-2026 returns only this configuration. This record identifies packages by UPC 787302130443 rather than by NDC.

Namespace context: the Class II index (213 records) and the recall hub (250 records, 118 FDA events); Gasco Industrial Corp. (6 indexed records) aggregates this firm across datasets.

Coverage and limits of this record

This page reflects the openFDA enforcement report for D-0665-2026 as ingested on 2026-08-22, which can lag the live FDA record and omits detail held only in primary documents. It offers no clinical assessment, no advice about whether to use any product, and no substitute. For any health question consult a qualified healthcare professional.

Source & provenance

Official source
https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0665-2026%22
Source dataset
openFDA Drug Enforcement API
Publication date
2026-07-15
Ingested
2026-08-22
Record hash
514f3c1032e4b066

Verify every value against the official FDA source above. This site links to the regulator's record rather than replacing it.