International safety notice
MAHURKAR Acute Triple Lumen Catheter; MAHURKAR Acute Dual Lumen Catheter; Argyle Acute Single Lumen Catheter. Priority 2 – Warning
Ireland / HPRA · IRL · May 21, 2019
Key facts
| Title | MAHURKAR Acute Triple Lumen Catheter; MAHURKAR Acute Dual Lumen Catheter; Argyle Acute Single Lumen Catheter. Priority 2 – Warning |
|---|---|
| Regulator | Ireland / HPRA |
| Country | IRL |
| Brand | MAHURKAR Acute Triple Lumen Catheter; MAHURKAR Acute Dual Lumen Catheter; Argyle Acute Single Lumen Catheter |
| Models | X13.5CM, 8888135198, 8888135137, 353-1-6764971, COMPONENTS-11.5FR, 8888115162, 8813817009, 8888101001HP, 8888115132, 8817277007, 8888340629, 8831663002 and 138 more |
| Event type | Safety Notice |
| Date | May 21, 2019 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1