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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/Prescription Drugs

Bryant Ranch Lidocaine Patch 5% Recalled for Labeling Error

Agency Publication Date: April 28, 2023
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Summary

Bryant Ranch Prepack, Inc. is voluntarily recalling 403 boxes of Lidocaine Patch 5% (lidocaine) because the packaging incorrectly identifies the medication as a tablet. A typographical error on the box and the individual patch labels states "each tablet contains" instead of "each adhesive patch contains." The recall involves 30-count cartons and the individual patches within those cartons distributed nationwide.

Risk

The labeling error incorrectly identifies the dosage form as a tablet, which could lead to confusion regarding how to properly use the medication. No injuries or adverse events related to this typographical error have been reported.

What You Should Do

  1. This recall affects Bryant Ranch Prepack Lidocaine Patch 5% (lidocaine) distributed in 30-count cartons (NDC 63629-8755-1) and individual 1-count patch packets (NDC 63629-8755-20).
  2. Identify the affected product by looking at the upper left-hand side of the outer box or individual patch label for the incorrect statement "each tablet contains" instead of "each adhesive patch contains."
  3. Check the lot number and expiration date printed on the packaging. Over 30 specific lot numbers are affected with expiration dates between September and December 2024. See the Affected Products section below for the full list of affected codes.
  4. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  5. 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 Patch 5% (30-count carton)
Variants: 5%, 700 mg, Adhesive Patch
Lot Numbers:
204603 (Exp: 09/30/2024)
208608 (Exp: 12/31/2024)
208749 (Exp: 12/31/2024)
208445 (Exp: 12/31/2024)
209101 (Exp: 12/31/2024)
208609 (Exp: 12/31/2024)
208295 (Exp: 12/31/2024)
209106 (Exp: 12/31/2024)
209102 (Exp: 12/31/2024)
209212 (Exp: 12/31/2024)
208975 (Exp: 12/31/2024)
209211 (Exp: 12/31/2024)
209706 (Exp: 12/31/2024)
209779 (Exp: 12/31/2024)
209624 (Exp: 12/31/2024)
209839 (Exp: 12/31/2024)
209548 (Exp: 12/31/2024)
204604 (Exp: 11/30/2024)
204601 (Exp: 11/30/2024)
204550 (Exp: 11/30/2024)
204599 (Exp: 11/30/2024)
204871 (Exp: 11/30/2024)
204555 (Exp: 11/30/2024)
205616 (Exp: 11/30/2024)
205612 (Exp: 10/31/2024)
204832 (Exp: 10/31/2024)
205127 (Exp: 10/31/2024)
204996 (Exp: 10/31/2024)
205615 (Exp: 10/31/2024)
205324 (Exp: 10/31/2024)
205494 (Exp: 10/31/2024)
205611 (Exp: 10/31/2024)
206232 (Exp: 10/31/2024)
NDC:
63629-8755-20
63629-8755-1

Relabeled by Bryant Ranch Prepack, Inc. Carton contains 30 patches.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92161
Status: Active
Manufacturer: Bryant Ranch Prepack, Inc.
Sold By: Pharmacies
Manufactured In: United States
Units Affected: 403 boxes
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.