Coons Interventional Wire Guide
Reported: March 21, 2018 Initiated: October 13, 2017 #Z-0954-2018
Product Description
Coons Interventional Wire Guide
Reason for Recall
Label does not state that the product is heparin-coated.
Details
- Recalling Firm
- Cook Inc.
- Units Affected
- 3,369
- Distribution
- Nationally
- Location
- Bloomington, IN
Frequently Asked Questions
What product was recalled? ▼
Coons Interventional Wire Guide. Recalled by Cook Inc.. Units affected: 3,369.
Why was this product recalled? ▼
Label does not state that the product is heparin-coated.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 21, 2018. Severity: Moderate. Recall number: Z-0954-2018.
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