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How to determine if your Duragesic® patch has been recalled

Source | FDA
DURAGESIC® (fentanyl transdermal system CII) Recall Notice Product Photos

Janssen Pharmaceutica Products, L.P., recalled one lot of DURAGESIC® (fentanyl transdermal system CII) 75 mcg per hour patches, control number 0327192. No other dosage strengths and lot numbers were affected. A control number is listed on every DURAGESIC® 75 mcg per hour on every patch carton and patch pouch. See the photos below for the location of the control number and dosage strength.

Photo of DURAGESIC 75 mcg/hr product carton
Photo of DURAGESIC 75 mcg/hr product carton

Only DURAGESIC 75 mcg/hr with Control number 0327192 are being recalled

 

DURAGESIC 75 mcg/hr product carton
DURAGESIC 75 mcg/hr product carton

 

Photo of DURAGESIC 75 mcg/hr product patch pouch
Photo of DURAGESIC 75 mcg/hr product patch pouch

 

DURAGESIC 75 mcg/hour patch
DURAGESIC 75 mcg/hour patch

 

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