Philips OmniWire Pressure guide wire recall
Philips OmniWire Pressure guide wire REF 89185J PN 300000252891
Why was Philips OmniWire Pressure guide wire recalled?
Due to a potential failed sterilization process.
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?
Model Number: 89185J Part Number: 300000252891 UDI Code: (01)00845225003050(11)220309(17)250309(10)0302535768 Serial Numbers: 37583 37586 37590 37598 37612 37648 37655 37692 37694 37709 37719
- Product
- Philips OmniWire Pressure guide wire REF 89185J PN 300000252891
- Recalling firm
- Volcano Corp
- Quantity
- 11 devices
- Distribution
- U.S.: WA and WI O.U.S.: Canada
- Recall date
- June 22, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)