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High risk Drugs & MedicationsClass II

IntegraDose Fentanyl Citrate Injection Recall

FentaNYL Citrate, Sterile CADD for Injection, 2,2500 mcg/50mL in Sterile Water, IntegraDose Compounding Services LLC, 3650 Victorie St N, Su

Updated May 12, 2026

IntegraDose Compounding Services is recalling fentanyl citrate sterile injection (2,500 mcg/50mL) because the doses are subpotent, meaning they contain less active medication than labeled. This can lead to inadequate pain relief or serious complications in patients who depend on accurate fentanyl dosing.

Is the IntegraDose Compounding Services LLC recalled? Yes. This product was recalled by FDA on May 12, 2026. Details below.

What is recalled

Fentanyl Citrate, Sterile CADD for Injection, 2,500 mcg/50mL in Sterile Water, NDC 71139-6030-1, manufactured by IntegraDose Compounding Services LLC, 3650 Victorie Street N, Suite 900, Shoreview, MN.

Am I affected

You are affected if you have been prescribed or administered fentanyl citrate sterile injection with NDC number 71139-6030-1 and concentration of 2,500 mcg/50mL in Sterile Water from IntegraDose Compounding Services.

What to do right now

Do not use this fentanyl product. Contact your healthcare provider or pharmacist immediately to obtain a replacement from a verified source and to discuss any doses you may have already received.

The hazard

Subpotent Drug

Brands affected

IntegraDose Compounding Services LLC
Source
FDA
Category
Drugs & Medications
Recall ID
fda-D-0548-2026
Classification
Class II
Recalled
May 12, 2026
Read the official notice

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