FDA recall record

Pharmedium Services fentaNYL Citrate, 10 mcg per 1 mL, in 0.9% Sodium Chloride, Preservative recall — FDA D-0093-2017

Subpotent Drug: confirmed subpotency in one lot of this product that was packaged and stored in syringes.

Class Iclassification
D-0093-2017official record ID
Oct 19, 2016report date

Recall record at a glance

Official recordD-0093-2017
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmPharmedium Services, LLC
Report dateOct 19, 2016
Recall initiation dateJul 17, 2015
Quantity500 syringes
LocationLake Forest, IL, United States

Official product description

fentaNYL Citrate, 10 mcg per 1 mL, in 0.9% Sodium Chloride, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3174.

Why the product was recalled

Subpotent Drug: confirmed subpotency in one lot of this product that was packaged and stored in syringes.

Distribution information

Nationwide

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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