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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Nephron Albuterol Sulfate Inhalation Solution Recalled for Illegible Labels

Agency Publication Date: April 14, 2026
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Summary

Nephron SC, LLC is recalling 146,280 vials of Albuterol Sulfate Inhalation Solution (0.5%, 25 mg/5 mL) because the labels on the vials are illegible. This recall affects sterile unit-dose vials distributed nationwide to hospitals, clinics, and pharmacies. No incidents or injuries have been reported to date, but the illegible labeling could lead to medication errors.

Risk

The labels on the individual vials cannot be clearly read, which may result in a patient or healthcare provider administering the wrong medication or the incorrect dosage.

What You Should Do

  1. If you have health concerns, contact your healthcare provider or pharmacist.
  2. Check your medication for Albuterol Sulfate Inhalation Solution, 0.5% (25 mg/5 mL) in 5 mL vials with lot number AB6001 and an expiration date of 1/15/2027.
  3. Return any unused product to the place of purchase for a refund, throw it away, or contact Nephron SC, LLC for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Albuterol Sulfate Inhalation Solution, 0.5%, 25 mg/5 mL (5 mg/mL*)
Variants: 30x5 mL Sterile Unit-Dose Vials, Rx only
Lot Numbers:
AB6001 (Exp 1/15/2027)
NDC:
69374-330-05

Manufactured at Nephron 503B Outsourcing facility, 4600 12th Street Extension, West Columbia, SC 29172.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98596
Status: Active
Manufacturer: Nephron SC, LLC
Sold By: nephron 503B Outsourcing facility; hospitals; clinics; pharmacies
Manufactured In: United States
Units Affected: 146,280
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.