[Recalled] Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Codes: ASK-42703-PTJH and ASK-45703-PTJH — Product sterility may be com
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Codes: ASK-42703-PTJH and ASK-45703-PTJH |
|---|---|
| Brand / manufacturer | Arrow International Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1997-2018 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 11 April 2018 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Product sterility may be compromised due to unsealed packaging.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Arrow International Inc
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.