Class I
Terminated
Lidocaine HCl Injection, USP, 2%, 20 mg per mL, Preservative-Free, 5 mL Single-Dose Vial, Rx only, For Infiltration and Nerve Block including Epidural and Caudal, Manufactured by: Hospira, Inc., Lake Forest, IL, 60045, NDC 0409-2066-05
This recall has been terminated (originally issued October 22, 2014).
- Company
- Hospira Inc.
- Recall Initiated
- July 29, 2014
- Posted
- October 22, 2014
- Recall Number
- D-0020-2015
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 109,110 Vials
- Firm Location
- Lake Forest, IL, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Presence of Particulate Matter: The product was discolored and contained visible particulates (iron oxide) in the solution and embedded in the glass vial.
Distribution
Nationwide
Lot / Code Info
Lot Number: 25-550-DD, Exp: 1JAN2015
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