FDA recall record

BayCare Integrated Service Center, LLC /dba Norepinephrine bitartrate 16 mg in 250 mL NaCl recall — FDA D-0569-2022

Subpotent drug

Class IIIclassification
D-0569-2022official record ID
Mar 2, 2022report date

Recall record at a glance

Official recordD-0569-2022
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmBayCare Integrated Service Center, LLC /dba BayCare Central Pharmacy
Report dateMar 2, 2022
Recall initiation dateFeb 14, 2022
Quantity1157 bags
LocationTemple Terrace, FL, United States

Official product description

Norepinephrine bitartrate 16 mg in 250 mL NaCl 0.9%, packaged in IV bags, Rx only, BayCare Central Pharmacy 7802 E. Telecom Parkway Temple Terrace, FL 33637 (813) 901-6392

Why the product was recalled

Subpotent drug

Distribution information

Florida

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken 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.

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