FDA recall record

Lidocaine HCl Injection, USP, 2%, 20 mg per mL recall — FDA D-1278-2014

Presence of Particulate Matter- Confimed customer complaint of particulates embedded in glass container and in contact with product solution.

Class Iclassification
D-1278-2014official record ID
May 7, 2014report date

Recall record at a glance

Official recordD-1278-2014
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmHospira Inc.
Report dateMay 7, 2014
Recall initiation dateDec 23, 2013
Quantity68,350 vials
LocationLake Forest, IL, United States

Official product description

Lidocaine HCl Injection, USP, 2%, 20 mg per mL, packaged in 5-mL single-dose vials, 10 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL. 60045, NDC 0409-2066-05.

Why the product was recalled

Presence of Particulate Matter- Confimed customer complaint of particulates embedded in glass container and in contact with product solution.

Distribution information

Nationwide

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: Press Release.

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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