Lidocaine HCl Injection recall: Particulate Matter
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 was Lidocaine HCl Injection recalled?
Presence of Particulate Matter- Confimed customer complaint of particulates embedded in glass container and in contact with product solution.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot 32135DD; Exp 08/15
- Product
- 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.
- Recalling firm
- Hospira Inc.
- Quantity
- 68,350 vials
- Distribution
- Nationwide
- Recall date
- May 7, 2014
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)