Inter-Med Llc: Medical Device Recall in 2019 - (Recall #: Z-0017-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Vista Dental Products Chlor-XTRA - 12mL Prefilled Syringes, QTY: 8, REF 503850

Product Classification:

Class II

Date Initiated: June 27, 2019

Date Posted: October 9, 2019

Recall Number: Z-0017-2020

Event ID: 83435

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.

Status: Terminated

Product Quantity: 384 units

Code Information:

Lot/Work Order Numbers: 2018-1471 2018-1992 20182211, UDI (01)10818207020502 20182779, UDI (01)10818207020502 20190041, UDI (01)10818207020502 20190309, UDI (01)10818207020502

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated