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Duragesic Patch Attorney and Fentanyl Lawyer for Duragesic Recall

Duragesic® Defective Drug Lawyers

The law firm of MacDonald Rothweiler Eisenberg L.L.P. was established to provide aggressive legal representation to individuals and their loved ones who have suffered serious injury or death. We have earned a reputation among the foremost personal injury attorneys in the Boston and Philadelphia areas as one of the most successful and talented plaintiff's firms. With over 100 years of combined experience, our renowned attorneys have achieved record-breaking results for our clients in cases against large insurance and other Fortune 500 companies.

Our legal team delivers the expertise, personal attention, and results our valued clients deserve throughout their important case. Our offices are located in Boston, Massachusetts and Philadelphia, Pennsylvania and Cherry Hill, New Jersey. MacDonald Rothweiler Eisenberg L.L.P. receives client referrals from many respected attorneys, who recognize us as among the most accomplished and professional legal advocates in the pharmaceutical products, personal injury, mass tort, medical malpractice, automobile "crashworthiness" and complex product liability fields.

Duragesic® Pain Patch Recall
On February 17, 2004, Janssen Pharmaceutica Products LP ("Janssen") issued, with the approval of the U.S. Food & Drug Administration (FDA) a Class I Recall of all units of its 75mcg/hr Duragesic® product bearing a specific lot number. Later on April 5, 2004, Janssen issued another urgent recall to include additional lot numbers that also may have contained defective Duragesic® patches. That product is manufactured for Janssen by Alza Corporation ("alza"). Both Janssen and Alza are wholly owned subsidiary companies of Johnson & Johnson.

Duragesic®, known as a "pain patch," is an adhesive patch applied to the tothe skin which is intended to deliver a steady dose of a powerful opioid pain medication (fentanyl) through the skin over an extended time to persons suffering from chronic and/or debilitating pain.

The fentanyl recall itself applies only to specific manufacturing lots of the 75mcg strength product, which (according to recall notices) were designed with a faulty seal which permits full strength fentanyl to leak from the patch delivery system. If the leakage occurs while the patch is on the skin, patients arepotentially caused to suffer an overdose of fentanyl which can result in fatal respiratory and/or cardiac arrest or other, serious physical reactions. The Duragesic® Patch litigation in which MacDonald Rothweiler Eisenberg LLP has taken a leading role, involves re-called patches and other Duragesic patches that are suspected of leaking fentanyl leading to the death of our clients due to "fentanyl toxicity." This may lead to a Duragesic lawsuit.

The lot number of the can be identified by its NDC number and Lot Control Number as follows:

NDC no. 50458-035-05

Lot Control nos. 0327192, 0327193, 0327294, 0327295, and 0330362

To determine whether your Duragesic® product is subject to this recall, please review these Duragesic® photos provided by Janssen to the FDA, which will direct you to the proper place to look for your Lot Control Number. If you cannot read the numbers accurately, a fentanyl patch attorney in our office may be able to better assist you.

If you or a loved one has suffered a catastrophic injury, which you believe is related to your use of a defective Duragesic™ patch, contact a Duragesic lawyer at MacDonald Rothweiler Eisenberg, LLP. to assess your potential legal claim.

Use the form below to contact us for our expert advice.

 
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Recall of Certain
Duragesic®Patches

Janssen Pharmaceutica is recalling one lot of DURAGESIC transdermal patches. The patches deliver the opioid fentanyl, used to treat severe chronic pain. A small percentage of the patches in this lot may leak medication because of an improper seal along one edge of the patch.

Duragesic®Recall Notice

Janssen Pharmaceutica Products, LP would like to inform you of a Class I Recall to users for
DURAGESIC@(fentanyltransdermal system) 75 mcg/h, NDC #50458-035-05, Control Number
0327192 (expiration October 2005).

Duragesic®Recall Notice

Janssen Pharmaceutica is recalling one lot of DURAGESIC® (fentanyl transdermal system CII) 75 mcg per hour patches, control number 0327192 , due to a potential leak in the product seal in a small percentage of patches in this one control number. Only this dosage strength and control number are affected.

 
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