FDA Enforcement Class II Terminated

Vista Dental Products Sodium Hypochlorite - 6%, QTY: 12, 3mL Pre-filled Syringes, REF 502350

Recall: Z-0014-2020 · Reported October 9, 2019

Enforcement

Recall Number
Z-0014-2020
Event ID
83435
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Inter-Med Llc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
October 9, 2019
Initiation Date
June 27, 2019
Classification Date
October 1, 2019
Termination Date
August 10, 2021
Address
2200 Northwestern Ave, N/A, Racine, WI, 53404-2500, United States

Description

Vista Dental Products Sodium Hypochlorite - 6%, QTY: 12, 3mL Pre-filled Syringes, REF 502350

Reason

The affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prolonged storage and exposure to contained solutions, the rubber bung may degrade due to chemical interaction with the bleach solution.

Code Info

UDI (01)10818207020458 Lot/Work Order Numbers: 20190197 20190723 20190834 20190862 20190952

Distribution

US, South Africa, Switzerland, Poland, Italy, Singapore, Australia

Quantity

768 units