Coons Interventional Wire Guide recall
Coons Interventional Wire Guide
Why was Coons Interventional Wire Guide recalled?
Label does not state that the product is heparin-coated.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Catalog # THSF-/-COONS-BH Affected lot codes range from: 3730001 - 6164916 F3729969 - F4922979 NS4928020 - NS6203182
- Product
- Coons Interventional Wire Guide
- Recalling firm
- Cook Inc.
- Quantity
- 3,369
- Distribution
- Nationally
- Recall date
- March 21, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)