Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters. Permits venous access and catheter introduction to the central circulation.
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Recall
- Recall Number
- Z-1158-2018
- Event Number
- 79342
- Firm
- Arrow International Inc
- FEI Number
- 3015859709
- Product Code
- DYB
- Status
- Terminated
- Root Cause
- Labeling mix-ups
- Initiated
- November 14, 2017
- Posted
- March 5, 2018
- Terminated
- July 15, 2019
- Address
- 2400 Bernville Rd, Reading, PA, 19605-9607
Description
Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters. Permits venous access and catheter introduction to the central circulation.
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.
On November 16, 2017, an Urgent Medical Device Notification titled "ARROW PSI and Pressure Injectable Multi-Lumen CVC Kits" was issued to customers informing them of the issue, and urging all to take the following actions: 1. Place a copy of this notification and the enclosed Central Line Insertion Checklist with each unit of affected product currently in your inventory. 2. Complete the enclosed Acknowledgement Form and fax it to 1-855-419-8507, Attn: Customer Service or e-mail to [email protected]. If you have any other questions, feel free to contact your local sales representative or Customer Service at 1-866-246-6990.
Nationwide Distribution
18,124 total