Rusch EasyCath Kit
Reported: August 7, 2019 Initiated: July 1, 2019 #Z-2086-2019
Product Description
Rusch EasyCath Kit
Reason for Recall
Potential for product not to be sterile.
Details
- Recalling Firm
- Teleflex Medical
- Units Affected
- 3,700 devices
- Distribution
- Nationwide distribution to CA, FL, IL, NC, NJ, OH, OK, TX.
- Location
- Morrisville, NC
Frequently Asked Questions
What product was recalled? ▼
Rusch EasyCath Kit. Recalled by Teleflex Medical. Units affected: 3,700 devices.
Why was this product recalled? ▼
Potential for product not to be sterile.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 7, 2019. Severity: Moderate. Recall number: Z-2086-2019.
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