FDA recall Z-0016-2020

Inter-Med Llc · Class II · device

Product

Vista Dental Products Chlor-XTRA - 3mL Prefilled Syringes, QTY: 12, REF 503825

Reason for recall

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.

Distribution

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

Key facts

Status
Terminated
Initiation date
2019-06-27
Report date
2019-10-09
Termination date
2021-08-10
Voluntary/Mandated
Voluntary: Firm initiated
Location
Racine, WI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0016-2020