Buffered Lidocaine recall: Labeling Error
Buffered Lidocaine, 1%, In Sodium Bicarbonate 8.4%, 1 mL Total Volume in a 3 mL syringe, Local anesthetic use, Rx only, PharMEDium, Product code…
Why was Buffered Lidocaine recalled?
Labeling; Label Mixup; outer packaging is incorrectly labeled as Buffered Lidocaine 1% instead of correctly as Buffered Lidocaine 0.9%
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 Numbers: 170110030M, 170110029M and 170070058M
- Product
- Buffered Lidocaine, 1%, In Sodium Bicarbonate 8.4%, 1 mL Total Volume in a 3 mL syringe, Local anesthetic use, Rx only, PharMEDium, Product code…
- Recalling firm
- Pharmedium Services, LLC
- Quantity
- 3879 syringes
- Distribution
- Nationwide
- Recall date
- March 22, 2017
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)