Recall Atlas
Drugs & medicalClass II

Mayne Pharma Inc recalls Clonidine Transdermal System, USP 0.3 mg/day, 4 Patches (NDC 51862-455-01) per Carton (51862-455-04), Rx only, Manufactured for: Mayne…

Defective Delivery System: Out of specification for release liner removal force results at the 3-month CRT stability timepoint.

Read the official notice →
Date
2022-06-29
Country
United States
Brand
Mayne Pharma
Product
Clonidine Transdermal System, USP 0.3 mg/day, 4 Patches (NDC 51862-455-01) per Carton (51862-455-04), Rx only, Manufactured for: Mayne…
Classification
Class II
Units
Nationwide in the US Market
Category
Drugs & medical
Source
FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

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    FDA · DrugMayne Pharma IncNationwide within the United StatesOfficial notice →
All 2 Mayne Pharma recalls →

Other drugs & medical recalls in the United States

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