FDA recall record

Metoclopramide Injection, USP 10 mg (5mg/mL), 2 mL Single-dose Vial recall — FDA D-012-2014

Presence of Particulate Matter: Potential vendor glass issue - glass spiticules (glass strands) were identified during site inspection of the vials.

Class IIclassification
D-012-2014official record ID
Nov 27, 2013report date

Recall record at a glance

Official recordD-012-2014
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmHospira Inc.
Report dateNov 27, 2013
Recall initiation dateSep 24, 2013
Quantity251,400 vials
LocationLake Forest, IL, United States

Official product description

Metoclopramide Injection, USP 10 mg (5mg/mL), 2 mL Single-dose Vial, Rx Only, Sterile, Hospira Inc., Lake Forest, IL, 60045, USA, NDC 0409-3414-01

Why the product was recalled

Presence of Particulate Matter: Potential vendor glass issue - glass spiticules (glass strands) were identified during site inspection of the vials.

Distribution information

Nationwide 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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