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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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Low RiskFDA Drug
Medications & Supplements/Topical Products

CVS Health Lidocaine Wound Gel Recalled for Failed pH Specifications

Agency Publication Date: April 30, 2026
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Summary

Water-Jel Technologies, LLC is recalling 31,488 tubes of CVS Health Lidocaine Wound Gel (Lidocaine Hydrochloride, 2% and Benzalkonium Chloride, 0.13%) because the product failed pH testing specifications. The recall affects 0.5 oz tubes distributed nationwide to CVS Pharmacy locations. Consumers should check their medicine cabinets for this topical gel and consult a healthcare professional if they have used it and have concerns.

Risk

The product does not meet the required acidity (pH) levels set for this medication, which can affect the drug's stability, effectiveness, and potentially cause skin irritation during use.

What You Should Do

  1. Check your Lidocaine Wound Gel packaging for lot numbers A5014, A5018, or A5019 and NDC 59898-950.
  2. If you have health concerns, contact your healthcare provider or pharmacist.
  3. Return any unused product to the place of purchase for a refund, throw it away, or contact Water-Jel Technologies, 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: Lidocaine Wound Gel (0.5 oz)by CVS Pharmacy
Variants: Benzalkonium Chloride, 0.13%, Lidocaine Hydrochloride, 2%
Lot Numbers:
A5014
A5018
A5019
NDC:
59898-950

Distributed by CVS Pharmacy, Inc.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98737
Status: Active
Manufacturer: Water-Jel Technologies, LLC
Sold By: CVS Pharmacy
Manufactured In: United States
Units Affected: 31,488
Distributed To: Nationwide

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.