MAHURKAR catheter kits recall in Canada: incorrect priming volumes
In plain language
This recall involves various MAHURKAR catheter kits sold in Canada. They are being recalled because the printed priming volumes on the catheters and instructions for use may be inaccurate. This could lead to incorrect locking volumes being used.
What to do
- Stop using the product immediately.
- Check model numbers if provided.
- Follow the return or repair instructions from the official notice.
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Affected products
MAHURKAR PC Kit
Model: 8888115132, 8888115162, 8888115192, 8888115242, 8888135133, 8888135163, 8888135193, 8888135243
Lot: All lots.
MAHURKAR QPlus SE Kits
Model: 8888135131, 8888135161, 8888135191, 8888135241
Lot: All lots.
MAHURKAR Acute High Pressure Triple Lumen Catheter Kit Curved Extensions
Model: 8888345603HP, 8888345611HP, 8888345629HP, 8888345637HP
Lot: All lots.
MAHURKAR Acute High Pressure Triple Lumen Catheter Kit Straight Extensions
Model: 8888340629HP, 8888340637HP
Lot: All lots.
MAHURKAR Acute Dual Lumen Catheter Kit Pre-Curved
Model: 8888115132, 8888115162, 8888115192, 8888115242, 8888135133, 8888135163, 8888135193, 8888135243
Lot: All lots.
MAHURKAR Acute Dual Lumen Catheter
Model: 8813-816009, 8813794005, 8813794009, 8813816005, 8817-142005, 8817145005, 8830-414001, 8830414002, 8831-662001, 8832-539001, 8832-539002, 8832-539003
Lot: All lots.
MAHURKAR Acute Dual Lumen Catheter Kits
Model: 8813-793009, 8813-793013, 8813-817005, 8813-817009, 8817-143005, 8817146001, 8817146007, 8817149007, 8830-415001, 8830-415003, 8831-173011, 8831173010, 8831661001, 8832539006, 8832539007
Lot: All lots.
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: All lots.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 8813-793009, 8813-793013, 8813-816009, 8813-817005, 8813-817009, 8813794005, 8813794009, 8813816005, 8817-142005, 8817-143005, 8817145005, 8817146001, 8817146007, 8817149007, 8830-414001, 8830-415001, 8830-415003, 8830414002, 8831-173011, 8831-662001, 8831173010, 8831661001, 8832-539001, 8832-539002, 8832-539003, 8832539006, 8832539007, 8888115132, 8888115162, 8888115192, 8888115242, 8888135131, 8888135133, 8888135161, 8888135163, 8888135191, 8888135193, 8888135241, 8888135243, 8888340629HP, 8888340637HP, 8888345603HP, 8888345611HP, 8888345629HP, 8888345637HP
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
This recall involves various MAHURKAR catheter kits sold in Canada. They are being recalled because the printed priming volumes on the catheters and instructions for use may be inaccurate. This could lead to incorrect locking volumes being used.
What should consumers do?
Stop using the product immediately. Check model numbers if provided. Follow the return or repair instructions from the official notice.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on June 7, 2019.
Is the MAHURKAR brand affected by this recall?
Yes, MAHURKAR products are affected by this recall. This recall involves various MAHURKAR catheter kits sold in Canada. They are being recalled because the printed priming volumes on the catheters and instructions for use may be inaccurate. This could lead to incorrect locking volumes being used.