RHONDIUM LIMITED: Medical Device Recall in 2019 - (Recall #: Z-0708-2020)

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:

Rhondium OVC3 One Visit Crown, Model FDI 24/25L USA 12/13L A2 HT, Nonsterile, Rx. The firm name on the label is Rhondium Ltd., Katikati, New Zealand.

Product Classification:

Class II

Date Initiated: January 31, 2019

Date Posted: December 25, 2019

Recall Number: Z-0708-2020

Event ID: 84126

Reason for Recall:

The product was mislabeled with an incorrect expiration date.

Status: Completed

Product Quantity: 6 devices

Code Information:

Lot numbers 1832-1099 and 1828-0982.

Distribution Pattern:

Distribution was made to IL, NM, TX, and WI. There was no foreign/military/government distribution.

Voluntary or Mandated:

Voluntary: Firm initiated