VersaSafe Plastic Cannula - 11 Gauge, Model 9391-0200 Product Usage: Used with secondary IV sets or syringes with a female luer lock adapter to administer fluid and medications through a needle or catheter inserted into a patients artery or vein.
Reported: August 23, 2017 Initiated: June 30, 2017 #Z-3030-2017
Product Description
VersaSafe Plastic Cannula - 11 Gauge, Model 9391-0200 Product Usage: Used with secondary IV sets or syringes with a female luer lock adapter to administer fluid and medications through a needle or catheter inserted into a patients artery or vein.
Reason for Recall
Punctures in blister packaging that was detected during the packaging process.
Details
- Recalling Firm
- CareFusion 303, Inc.
- Units Affected
- 1,546,800 units
- Distribution
- Worldwide Distribution in the states of : CO, IL, IN, MD, MI, NY, OH, & TX. and foreign countries of: Australia, New Zealand, & Japan.
- Location
- San Diego, CA
Frequently Asked Questions
What product was recalled? ▼
VersaSafe Plastic Cannula - 11 Gauge, Model 9391-0200 Product Usage: Used with secondary IV sets or syringes with a female luer lock adapter to administer fluid and medications through a needle or catheter inserted into a patients artery or vein.. Recalled by CareFusion 303, Inc.. Units affected: 1,546,800 units.
Why was this product recalled? ▼
Punctures in blister packaging that was detected during the packaging process.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 23, 2017. Severity: Moderate. Recall number: Z-3030-2017.
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