Database updated: 18 November 2024
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29931 |
| Brand Name: | Filter, bacteria, breathing circuit |
| Model: | 19212: ISO GARD filters. |
| Affected: | KMZ21C0564; KMZ21B1183, KMZ21C0908, KMZ20H0213, KMZ20H0705, KMZ20H1042, KMZ21B1062, KMZ21C1208, KMZ21D0018. |
| Software version: | |
| Recalling Organisation: | Teleflex Medical New Zealand PwC, Level 8, Pwc Tower 188 Quay Street Auckland 1010 |
| Contact Information: | 027 476 4009 |
| Manufacturer: | Teleflex Medical Sdn Bhd |
| Issue: | The manufacturer has become aware that the device splits or detaches during use. If this happens, the functionality and efficiency of the device may be compromised, potentially resulting in leakage and insufficient air supply to the patient with potential desaturation. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 8/9/2022 |
