VersaSafe Extension Set, Model No. 21000M-007
Reported: December 11, 2013 Initiated: November 8, 2013 #Z-0435-2014
Product Description
VersaSafe Extension Set, Model No. 21000M-007
Reason for Recall
CareFusion is recalling the VersaSafe Extension Intravascular Administration Set because it may have excessive adhesive which will prevent the male spin collar to operate as intended.
Details
- Recalling Firm
- CareFusion 303, Inc.
- Units Affected
- 3500 units
- Distribution
- Nationwide Distribution.
- Location
- San Diego, CA
Frequently Asked Questions
What product was recalled? ▼
VersaSafe Extension Set, Model No. 21000M-007. Recalled by CareFusion 303, Inc.. Units affected: 3500 units.
Why was this product recalled? ▼
CareFusion is recalling the VersaSafe Extension Intravascular Administration Set because it may have excessive adhesive which will prevent the male spin collar to operate as intended.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 11, 2013. Severity: Moderate. Recall number: Z-0435-2014.
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