FDA recall record

SODIUM CHLORIDE 0.45% Sodium Chloride Injection USP, 1000 mL recall — FDA D-407-2014

Labeling: Wrong Bar Code; Bar code scans as 0.15% Potassium Chloride in 0.9% Sodium Chloride (20 mEq K/liter).

Class IIclassification
D-407-2014official record ID
Jan 22, 2014report date

Recall record at a glance

Official recordD-407-2014
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmB. Braun Medical Inc.
Report dateJan 22, 2014
Recall initiation dateNov 27, 2013
Quantity19,572 bags
LocationIrvine, CA, United States

Official product description

0.45% Sodium Chloride Injection USP, 1000 mL. Rx only, Manufactured by B. Braun Medical Inc, 2525 McGaw Ave, Irvine, CA 92614. NDC 0264-7802-00.

Why the product was recalled

Labeling: Wrong Bar Code; Bar code scans as 0.15% Potassium Chloride in 0.9% Sodium Chloride (20 mEq K/liter).

Distribution information

Nationwide in the US and Puerto Rico.

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: Letter.

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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