| Type of Product |
Medical Device |
| TGA Recall Reference |
RC-2024-RN-00937-1 |
| Product Name/Description |
JuggerLoc/ToggleLoc 2.9mm Drill Guide
Product Code:110027357
Multiple item numbers, UDI numbers and lot numbers
ARTG 210279
(Zimmer Biomet Pty LtdPty Ltd - Arthroscopic access cannula kit) |
| Recall Action Level |
Wholesale |
| Recall Action Classification |
Class III |
| Recall Action Commencement Date |
25/10/2024 |
| Responsible Entity |
|
| Reason/Issue |
Zimmer Biomet is conducting a lot specific medical device recall for the JuggerLoc Disposable Cannula Kit - Drill Guide.
Zimmer Biomet has received multiple complaints globally where it was reported that the guides were discernibly warped when pulled out of packaging. Following investigation, the warping has been attributed to the cleaning process used during supplier manufacturing. |
| Recall Action |
Recall |
| Recall Action Instructions |
Customers should Immediately locate and quarantine all affected product. If customers identify affected stock, a Device Technologies representative will contact them upon receipt of the customer acknowledgement form to arrange the return and credit/replacement |
| Contact Information |
0400 480 202 - Anthony Sauer - Business Manager |