HIGHFDA DRUG

H-E-B inControl Alcohol Pads Recalled for Subpotent Isopropyl Alcohol (2025)

H-E-B and its inControl brand recall 300,000 sterile alcohol pads nationwide after the FDA alerted a subpotent isopropyl alcohol concentration. The pads were packaged in China with components from Taiwan and distributed nationwide. Consumers should stop using the product immediately and seek guidance from healthcare providers or MEDLINE INDUSTRIES, LP.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
July 7, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
July 7, 2025
Hazard Level
HIGH
Brands
H-E-B, inControl Alcohol
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
1 states
At-Risk Groups
GENERAL, PREGNANT, PETS

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
H-E-B, inControl Alcohol
Product type
Isopropyl Alcohol Pads
Model numbers
61224080041
UPC codes
37808-809, 37808-809-30, 37808-809-60, 37808-809-09, 6122408004
Sold at
Unknown
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    July 7, 2025

  2. Reported by FDA DRUG

    September 3, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact MEDLINE INDUSTRIES, LP - Northfield or your healthcare provider for guidance. Notification method: Letter

About This Product

Sterile alcohol pads are used to clean and disinfect small wounds or skin areas in medical settings and homes.

Why This Is Dangerous

Subpotent isopropyl alcohol means the antiseptic may not be as effective as labeled, potentially compromising disinfection.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Could affect the effectiveness of wound cleansing and infection prevention in clinical and home settings.

Practical Guidance

How to identify if yours is affected

  1. Check NDC 37808-809-09 on packaging and 61224080041 model number.
  2. Verify packaging origin: Packed in China with components from Taiwan.
  3. Confirm nationwide distribution if you have received shipments.

Where to find product info

FDA recall page D-0603-2025 for enforcement details.

What timeline to expect

Refunds or replacements coordinated via MEDLINE INDUSTRIES, LP; processing typically 4-6 weeks.

If the manufacturer is unresponsive

  • Document all communications
  • Escalate to MEDLINE supervisor or FDA consumer complaint
  • Consider filing a consumer complaint with FDA if unresolved.

How to prevent similar issues

  • Always verify NDC and lot numbers before using antiseptics.
  • Prefer products with verified potency and shelf-life labels.
  • Maintain inventory controls to track recalls.

Documentation advice

Keep recall notice, packaging, purchase receipts, and correspondence for records.

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

Product Details

Brand: H-E-B, inControl Alcohol. Product: Sterile Alcohol Pads, CONT. 100 PADS. Model: 61224080041. NDC: 37808-809-09. Packaging: 100 pads per containeR. Packaging location: Packaged in China with components from Taiwan. Sold nationwide.

Reported Incidents

No specific injuries or incidents are described in the recall notice. The hazard is categorized as HIGH.

Key Facts

  • Category: Health & Personal Care, Drugs & Medications

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERALPREGNANTPETSPREGNANT
Injury Types
OTHER

Product Details

Model Numbers
61224080041
UPC Codes
37808-809
37808-809-30
37808-809-60
+2 more
Affected States
ALL
Report Date
September 3, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

Related Recalls

Health & Personal Care
MEDIUM

AvKARE Recalls Rosuvastatin Tablets Due to Dissolution Issues

AvKARE recalled 7,991 cartons of Rosuvastatin Tablets on December 31, 2025. The recall stems from the product being out of specification for dissolution. Consumers should stop using the medication immediately and consult healthcare providers for guidance.

SUN PHARMACEUTICAL INDUSTRIES
Labeling: Not
Read more