PlainRecalls
FDA Drug Moderate Class II Terminated

0.9% Buffered Lidocaine HCl (buffered in 8.4% Sodium Bicarbonate) a.) 1 mL in 3 mL BD Syringe, 10 per carton, b.) 0.9% Buffered Lidocaine HCl (buffered in 8.4% Sodium Bicarbonate) 5 mL in 5 mL BD Syringe, 10 per carton Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478.

Reported: January 16, 2019 Initiated: January 2, 2019 #D-0374-2019

Product Description

0.9% Buffered Lidocaine HCl (buffered in 8.4% Sodium Bicarbonate) a.) 1 mL in 3 mL BD Syringe, 10 per carton, b.) 0.9% Buffered Lidocaine HCl (buffered in 8.4% Sodium Bicarbonate) 5 mL in 5 mL BD Syringe, 10 per carton Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478.

Reason for Recall

Subpotent

Details

Recalling Firm
PharMEDium Services, LLC.
Units Affected
7,711 syringes
Distribution
Product was distributed throughout the United States.
Location
Cleveland, MS

Frequently Asked Questions

What product was recalled?
0.9% Buffered Lidocaine HCl (buffered in 8.4% Sodium Bicarbonate) a.) 1 mL in 3 mL BD Syringe, 10 per carton, b.) 0.9% Buffered Lidocaine HCl (buffered in 8.4% Sodium Bicarbonate) 5 mL in 5 mL BD Syringe, 10 per carton Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478.. Recalled by PharMEDium Services, LLC.. Units affected: 7,711 syringes.
Why was this product recalled?
Subpotent
Which agency issued this recall?
This recall was issued by the FDA Drug on January 16, 2019. Severity: Moderate. Recall number: D-0374-2019.