FDA recall record

QuVa Pharma Norepinephrine 4 mg (16 mcg/mL) added to 5% Dextrose 250 mL Bag Preservative recall — FDA D-0003-2019

Subpotent Drug: Product may not have the active ingredient present in the bag.

Class Iclassification
D-0003-2019official record ID
Sep 26, 2018report date

Recall record at a glance

Official recordD-0003-2019
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmQuVa Pharma, Inc.
Report dateSep 26, 2018
Recall initiation dateAug 27, 2018
Quantity528 bags
LocationSugar Land, TX, United States

Official product description

Norepinephrine 4 mg (16 mcg/mL) added to 5% Dextrose 250 mL Bag Preservative Free, Rx only, QuVa Pharma, 519 Route 173, Bloombury, NJ 08804, UPC 70092103417.

Why the product was recalled

Subpotent Drug: Product may not have the active ingredient present in the bag.

Distribution information

Nationwide to hospitals in USA

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.