FDA recall record

Pharmedium Services remifentanil HCl, 50 mcg per mL, 100 mcg per 2 mL, in 0.9% Sodium recall — FDA D-0088-2017

Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.

Class IIclassification
D-0088-2017official record ID
Oct 19, 2016report date

Recall record at a glance

Official recordD-0088-2017
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPharmedium Services, LLC
Report dateOct 19, 2016
Recall initiation dateJul 17, 2015
Quantity1623 syringes
LocationLake Forest, IL, United States

Official product description

remifentanil HCl, 50 mcg per mL, 100 mcg per 2 mL, in 0.9% Sodium Chloride, Preservative Free, 2 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2R3300.

Why the product was recalled

Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.

Distribution information

Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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

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