Multi Lumen Central Venous Catheterization Kit; Product Code: ASK-12703-HH2; Exp. Dates Feb 2018 - Nov 2018
Reported: February 28, 2018 Initiated: October 17, 2017 #Z-0650-2018
Product Description
Multi Lumen Central Venous Catheterization Kit; Product Code: ASK-12703-HH2; Exp. Dates Feb 2018 - Nov 2018
Reason for Recall
These finished good kits may contain the incorrect Springwire Guide (SWG).
Details
- Recalling Firm
- Arrow International Inc
- Units Affected
- 5,926 total
- Distribution
- Distribution US Nationwide
- Location
- Reading, PA
Frequently Asked Questions
What product was recalled? ▼
Multi Lumen Central Venous Catheterization Kit; Product Code: ASK-12703-HH2; Exp. Dates Feb 2018 - Nov 2018. Recalled by Arrow International Inc. Units affected: 5,926 total.
Why was this product recalled? ▼
These finished good kits may contain the incorrect Springwire Guide (SWG).
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 28, 2018. Severity: Moderate. Recall number: Z-0650-2018.
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