PlainRecalls
FDA Drug Moderate Class II Terminated

LET Gel 4% (Lidocaine HCl 4% + EPINEPHrine HCl 0.05% + Tetracaine HCl 0.5%), 3mL Single Use Syringe, Rx only, US Compounding, 1270 Don's Lane, Conway, AR, 800-718-3588, Barcode 62295501303.

Reported: February 20, 2019 Initiated: January 24, 2019 #D-0482-2019

Product Description

LET Gel 4% (Lidocaine HCl 4% + EPINEPHrine HCl 0.05% + Tetracaine HCl 0.5%), 3mL Single Use Syringe, Rx only, US Compounding, 1270 Don's Lane, Conway, AR, 800-718-3588, Barcode 62295501303.

Reason for Recall

Labeling: Incorrect or Missing Lot and/or Exp Date: Labels are missing lot and expiration date and are printed as Lot# YYYDDYY@XX with a Beyond Use Date: MM/DD/YYY.

Details

Recalling Firm
US Compounding Inc
Units Affected
1931 syringes
Distribution
Nationwide in the USA.
Location
Conway, AR

Frequently Asked Questions

What product was recalled?
LET Gel 4% (Lidocaine HCl 4% + EPINEPHrine HCl 0.05% + Tetracaine HCl 0.5%), 3mL Single Use Syringe, Rx only, US Compounding, 1270 Don's Lane, Conway, AR, 800-718-3588, Barcode 62295501303.. Recalled by US Compounding Inc. Units affected: 1931 syringes.
Why was this product recalled?
Labeling: Incorrect or Missing Lot and/or Exp Date: Labels are missing lot and expiration date and are printed as Lot# YYYDDYY@XX with a Beyond Use Date: MM/DD/YYY.
Which agency issued this recall?
This recall was issued by the FDA Drug on February 20, 2019. Severity: Moderate. Recall number: D-0482-2019.