Mahurkar Acute Dual Lumen Catheter Tray, High Flow¿ Pre-Curved with IC* Safety Components, 13.5 FR x 13.5 cm Item Code: 8888135139 Product Usage: Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular access devices.
Reported: September 9, 2015 Initiated: August 6, 2015 #Z-2527-2015
Product Description
Mahurkar Acute Dual Lumen Catheter Tray, High Flow¿ Pre-Curved with IC* Safety Components, 13.5 FR x 13.5 cm Item Code: 8888135139 Product Usage: Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular access devices.
Reason for Recall
Sterility may be compromised
Details
- Recalling Firm
- Covidien LLC
- Units Affected
- 8 kits
- Distribution
- US Nationwide Distribution
- Location
- North Haven, CT
Frequently Asked Questions
What product was recalled? ▼
Mahurkar Acute Dual Lumen Catheter Tray, High Flow¿ Pre-Curved with IC* Safety Components, 13.5 FR x 13.5 cm Item Code: 8888135139 Product Usage: Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular access devices.. Recalled by Covidien LLC. Units affected: 8 kits.
Why was this product recalled? ▼
Sterility may be compromised
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 9, 2015. Severity: Moderate. Recall number: Z-2527-2015.
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