Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter, Catheter, Percutaneous The Arrow Single-Lumen Catheter permits venous access to the central circulation
Reported: June 21, 2017 Initiated: May 9, 2017 #Z-2328-2017
Product Description
Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter, Catheter, Percutaneous The Arrow Single-Lumen Catheter permits venous access to the central circulation
Reason for Recall
Arrow International is recalling the affected product because the packaging may not be completely sealed, which may compromise sterility.
Details
- Recalling Firm
- Arrow International Inc
- Units Affected
- 27,485 units distributed in U.S., 4,371 units distributed internationally
- Distribution
- Worldwide Distribution - US (nationwide) and Canada
- Location
- Reading, PA
Frequently Asked Questions
What product was recalled? ▼
Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter, Catheter, Percutaneous The Arrow Single-Lumen Catheter permits venous access to the central circulation. Recalled by Arrow International Inc. Units affected: 27,485 units distributed in U.S., 4,371 units distributed internationally.
Why was this product recalled? ▼
Arrow International is recalling the affected product because the packaging may not be completely sealed, which may compromise sterility.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 21, 2017. Severity: Moderate. Recall number: Z-2328-2017.
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