Femoral Artery Pressure Monitoring Set recall
Femoral Artery Pressure Monitoring Set
Why was Femoral Artery Pressure Monitoring Set 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 # C-PMS-300-CHILDRENS-A- 032988 ALL LOTS
- Product
- Femoral Artery Pressure Monitoring Set
- Recalling firm
- Cook Inc.
- Quantity
- 266
- Distribution
- Nationally
- Recall date
- March 21, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)