Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 16724 |
| Brand Name: | Baxter Minicap Extended Life PD Transfer Set with Twist Clmp |
| Model: | Product Codes: 5C4482, 5C4483, R5C4482, R5C4483, R5C4484 |
| Affected: | All lots |
| Software version: | |
| Recalling Organisation: | Baxter Healthcare Ltd 33 Vestey Drive Mt Wellington AUCKLAND |
| Contact Information: | 0800 229 837 |
| Manufacturer: | Baxter Healthcare Corporation |
| Brand Name: | Baxter Minicap, Opticap, Con Shield II transfer sets |
| Model: | SPC4486, SPC4211, R5C4484 |
| Affected: | All lots |
| Software version: | |
| Recalling Organisation: | Baxter Healthcare Ltd 33 Vestey Drive Mt Wellington AUCKLAND |
| Contact Information: | 0800 229 837 |
| Manufacturer: | Baxter Healthcare Corporation SA |
| Brand Name: | Baxter Minicap Extended Life PD Transfer Set |
| Model: | 5C4449, 5C4483, 5C4482X1, R5C4482, 5C4160, 5C4160X1 |
| Affected: | All lots |
| Software version: | |
| Recalling Organisation: | Baxter Healthcare Ltd 33 Vestey Drive Mt Wellington AUCKLAND |
| Contact Information: | 0800 229 837 |
| Manufacturer: | Baxter Healthcare Corporation |
| Brand Name: | Baxter Minicap Extended Life PD Transfer Set with Twist Clamp |
| Model: | 5C4482 |
| Affected: | All lots |
| Software version: | |
| Recalling Organisation: | Baxter Healthcare Ltd 33 Vestey Drive Mt Wellington AUCKLAND |
| Contact Information: | 0800 229 837 |
| Manufacturer: | Medigroup Inc |
| Brand Name: | Baxter Locking Titanium adapter for Peritoneal Dialysis |
| Model: | 5C4129, SPC4129ANZ |
| Affected: | All lots |
| Software version: | |
| Recalling Organisation: | Baxter Healthcare Ltd 33 Vestey Drive Mt Wellington AUCKLAND |
| Contact Information: | 0800 229 837 |
| Manufacturer: | Baxter Healthcare Corporation SA |
| Issue: | Baxter is adding a contraindication statement to address iodine allergy for Baxter's peritoneal dialysis products which contain iodine (i.e. povidone iodine) or for which iodine use is recommended. There have been no reports of complaints associated with these products for allergic or adverse reactions to iodine. Furthermore, this action is intended to ensure labelling consistency across the peritoneal dialysis portfolio |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 19/5/2014 |
