FDA Drug Recalls

Recalls / Class II

Class IID-1221-2019

Product

Lidocaine Buffered with J-Tip 0.25 mL, 1 mL syringe, 10:1, For Intradermal Use Only, Made by: Enterprise Pharmacy, 4400 Golf Acres Drive, Bldg. J Suite E, Charlotte, NC, 28208.

Affected lot / code info
Lots: ED041901 Exp. 4/13/2019; ED051901 Exp. 4/14/2019; ED081901 Exp. 4/17/2019; ED01901 Exp. 4/18/2019; ED101901 Exp. 4/19/2019; ED111901 Exp. 4/20/2019

Why it was recalled

Lack of sterility assurance.

Recalling firm

Firm
CMC Enterprise Pharmacy
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
4400 Golf Acres Dr, N/A, Charlotte, North Carolina 28208-5968

Distribution

Quantity
705 syringes
Distribution pattern
NC

Timeline

Recall initiated
2019-04-12
FDA classified
2019-04-23
Posted by FDA
2019-05-01
Terminated
2019-10-30
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1221-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls