FDA recall record

New England Life Care, Inc. dba Advanced Phenylephrine HCl 20 mg added to 0.9% Sodium recall — FDA D-0778-2023

Product Mix up; Product was compounded in 250 mL 5% Dextrose instead of 250 mL 0.9% Sodium Chloride

Class IIIclassification
D-0778-2023official record ID
Jun 7, 2023report date

Recall record at a glance

Official recordD-0778-2023
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmNew England Life Care, Inc. dba Advanced Compounding Solutions
Report dateJun 7, 2023
Recall initiation dateMay 22, 2023
Quantity198
LocationWoburn, MA, United States

Official product description

Phenylephrine HCl 20 mg added to 0.9% Sodium Chloride 250mL Bag, Rx Only, Compounded by: Advanced Compounding Solutions, 4 Constitution Way Ste L Woburn, Massachusetts 01801-1042 United States, NDC 71546-451-25

Why the product was recalled

Product Mix up; Product was compounded in 250 mL 5% Dextrose instead of 250 mL 0.9% Sodium Chloride

Distribution information

Nationwide in the USA.

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: 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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