5% Lidocaine HCL and 7.5% Dextrose Injection recall
5% Lidocaine HCL and 7.5% Dextrose Injection, USP, 2 mL Single-dose ampule, 5 count box, Rx Only, For Spinal Anesthesia Only, Manufactured by Hospira…
Why was 5% Lidocaine HCL and 7.5% Dextrose Injection recalled?
Failed Stability Specifications: The recalled lots did not meet the specification for color and pH throughout shelf life.
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 # 34-547-DK, 34-548-DK, Exp. 10/16, Lot # 39-372-DK, Exp. 03/17 Lot Number may be followed by numbers from 01 to 99
- Product
- 5% Lidocaine HCL and 7.5% Dextrose Injection, USP, 2 mL Single-dose ampule, 5 count box, Rx Only, For Spinal Anesthesia Only, Manufactured by Hospira…
- Recalling firm
- Hospira Inc.
- Quantity
- 287,200 2 mL ampules
- Distribution
- US and Puerto Rico
- Recall date
- December 14, 2016
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)