Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 23337 |
| Brand Name: | Turnpike and Turnpike LP Catheters |
| Model: | |
| Affected: | Turnpike LP 135CM - Lot number - 617381, Turnpike LP 150CM - Lot number - 616767 |
| Software version: | |
| Recalling Organisation: | Teleflex Medical New Zealand OFFICE 011, 110 CARLTON GORE ROAD Newmarket Auckland 1023 |
| Contact Information: | 027 476 4009 |
| Manufacturer: | Vascular Solutions LLC |
| Issue: | In the IFU specification table, the Turnpike LP distal shaft outer diameter is incorrectly listed as 0.86mm / 0.034" (2.6F) - the correct dimension is 0.74mm / 0.029" (2.2F). The box and pouch labels contain the correct dimensions. There is no risk of harm associated with use of these catheters. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 17/7/2018 |
