Pediatric Two-Lumen Central Venous Catheterization Set with Blue FlexTip Catheter (2018-11-12)
In plain language
This recall involves the Pediatric Two-Lumen Central Venous Catheterization Set with Blue FlexTip Catheter sold in Canada. It's being recalled because of a labelling error on the Lidstock that states incorrect priming volume and flow rates. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check model and lot numbers.
- Contact Arrow International for more information.
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Affected products
Pediatric Two-Lumen Central Venous Catheterization Set with Blue FlexTip Catheter
Model: CS-12402
Lot: 14F18E0121, 14F18F0336
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: 14F18E0121, 14F18F0336
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: CS-12402
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 the Pediatric Two-Lumen Central Venous Catheterization Set with Blue FlexTip Catheter sold in Canada. It's being recalled because of a labelling error on the Lidstock that states incorrect priming volume and flow rates. Stop using the product and follow the return steps in the official notice.
What should consumers do?
Stop using the product immediately. Check model and lot numbers. Contact Arrow International for more information.
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 December 10, 2018.
Is the Arrow International brand affected by this recall?
Yes, Arrow International products are affected by this recall. This recall involves the Pediatric Two-Lumen Central Venous Catheterization Set with Blue FlexTip Catheter sold in Canada. It's being recalled because of a labelling error on the Lidstock that states incorrect priming volume and flow rates. Stop using the product and follow the return steps in the official notice.