Pharmedium Services, LLC recalls Buffered Lidocaine, 1%, In Sodium Bicarbonate 8.4%, 1 mL Total Volume in a 3 mL syringe, Local anesthetic use, Rx only,…

Recall date

January 27, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0603-2017

FDA classification

Class III

Brand / firm

Pharmedium Services, LLC

Sold / distributed

Nationwide

Why it was recalled

Labeling; Label Mixup; outer packaging is incorrectly labeled as Buffered Lidocaine 1% instead of correctly as Buffered Lidocaine 0.9%

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

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 2K2466