Arrow International's various Central Venous Catheter Kits (2017-11-29)
In plain language
This recall involves various Arrow International Central Venous Catheter Kits sold in Canada. They are being recalled because some products may be missing a sticker with important lot number, expiration date, and Unique Device Identification (UDI) information. Stop using the product and follow the instructions in the official notice.
What to do
- Stop using the product immediately.
- Check the lot and model numbers if you have these products.
- Follow the instructions from your healthcare provider or the official notice for return or disposal.
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Affected products
ARROW-HOWES MULTI-LUMEN CENTRAL VENOUS CATHETERIZATION SET
Model: ASK-12703-PRJ, ASK15703-PRJ
Lot: 13F17B0265, 13F17B0279, 13F17D0112
ARROWG+ARD BLUE PLUS CENTRAL VENOUS CATHETER KITS
Model: ASK-42703-PRJ, ASK-45703-PRJ
Lot: 13F16L0007, 13F16M0013, 13F16M0019, 13F17A0296, 13F17B0343, 13F17D0110, 13F17D0113, 13F17F0319, 13F17G0059, 13F17H0095
AGB+ PRESSURE INJECTABLE MULTI-LUMEN CVC KIT
Model: CA-42703-P1A, CA-45703-P1A, CDA-42703-P1A, CDA-42802-P1A, CDA-45703-P1A, CDA-47702-P1A
Lot: 13F16K0239, 13F16K0306, 13F16L0091, 13F16L0092, 13F16L0285, 13F16M0047, 13F17A0022, 13F17A0157, 13F17A0167, 13F17A0301, 13F17B0117, 13F17B0145, 13F17B0152, 13F17B0249, 13F17C0057, 13F17C0174, 13F17C0250, 13F17C0266, 13F17C0318, 13F17C0466, 13F17D0039, 13F17E0095, 13F17F0259, 13F17F0261, 13F17F0298, 13F17F0299, 13F17G0090, 13F17G0541, 13F17H0068, 13F17H0071, 13F17H0096, 13F17H0100, 13F17H0566
AGB+ PRESSURE INJECTABLE QUAD-LUMEN CVC KIT
Model: CA-42854-P1A, CA-45854-P1A, CDA-42854-P1A, CDA-45854-P1A
Lot: 13F16K0302, 13F16L0071, 13F16M0048, 13F17C0325, 13F17D0283, 13F17E0124, 13F17F0071, 13F17F0497, 13F17F0748, 13F17G0428, 13F17H0387
PERCUTANEOUS SHEATH INTRODUCER KIT WITH ARROWG+ARD BLUE(R) SHEATH
Model: CDA-29803-1A
Lot: 13F16M0122, 13F17C0267, 13F17E0385, 13F17F0071, 13F17F0226, 13F17G0192, 13F17H0407
TWO-LUMEN CENTRAL VENOUS ACCESS KIT
Model: CDA-21242-1A
Lot: 13F16L0209, 13F17F0437, 13F17H0503
ARROWG+ARD BLUE LARGE BORE MULTI-LUMEN CVC KIT
Model: CDA-22123-1A
Lot: 13F17F0744
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: 13F16K0239, 13F16K0306, 13F16L0091, 13F16L0092, 13F16L0285, 13F16M0047, 13F17A0022, 13F17A0157, 13F17A0167, 13F17A0301, 13F17B0117, 13F17B0145, 13F17B0152, 13F17B0249, 13F17C0057, 13F17C0174, 13F17C0250, 13F17C0266, 13F17C0318, 13F17C0466, 13F17D0039, 13F17E0095, 13F17F0259, 13F17F0261, 13F17F0298, 13F17F0299, 13F17G0090, 13F17G0541, 13F17H0068, 13F17H0071, 13F17H0096, 13F17H0100, 13F17H0566, 13F16K0302, 13F16L0071, 13F16M0048, 13F17C0325, 13F17D0283, 13F17E0124, 13F17F0071, 13F17F0497, 13F17F0748, 13F17G0428, 13F17H0387, 13F16L0007, 13F16M0013, 13F16M0019, 13F17A0296, 13F17B0343, 13F17D0110, 13F17D0113, 13F17F0319, 13F17G0059, 13F17H0095, 13F16L0209, 13F17F0437, 13F17H0503, 13F16M0122, 13F17C0267, 13F17E0385, 13F17F0071, 13F17F0226, 13F17G0192, 13F17H0407, 13F17B0265, 13F17B0279, 13F17D0112, 13F17F0744
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: ASK-12703-PRJ, ASK-42703-PRJ, ASK-45703-PRJ, ASK15703-PRJ, CA-42703-P1A, CA-42854-P1A, CA-45703-P1A, CA-45854-P1A, CDA-21242-1A, CDA-22123-1A, CDA-29803-1A, CDA-42703-P1A, CDA-42802-P1A, CDA-42854-P1A, CDA-45703-P1A, CDA-45854-P1A, CDA-47702-P1A
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 Arrow International Central Venous Catheter Kits sold in Canada. They are being recalled because some products may be missing a sticker with important lot number, expiration date, and Unique Device Identification (UDI) information. Stop using the product and follow the instructions in the official notice.
What should consumers do?
Stop using the product immediately. Check the lot and model numbers if you have these products. Follow the instructions from your healthcare provider or the official notice for return or disposal.
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 January 8, 2018.
Is the Arrow International brand affected by this recall?
Yes, Arrow International products are affected by this recall. This recall involves various Arrow International Central Venous Catheter Kits sold in Canada. They are being recalled because some products may be missing a sticker with important lot number, expiration date, and Unique Device Identification (UDI) information. Stop using the product and follow the instructions in the official notice.