ViperWire Advance Peripheral Guide Wire recall
ViperWire Advance Peripheral Guide Wire, Sterilized with Ethylene Oxide, Rx Only. Part number 72023-02, Model Number VPR-GW-17. Five (5) guide wire…
Why was ViperWire Advance Peripheral Guide Wire recalled?
The pouch label was missing the use by date (UBD) of 2018-04.
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?
Lot #160877, UDI Number: (01)10852528005084(17)180430(10)160877.
- Product
- ViperWire Advance Peripheral Guide Wire, Sterilized with Ethylene Oxide, Rx Only. Part number 72023-02, Model Number VPR-GW-17. Five (5) guide wire…
- Recalling firm
- Cardiovascular Systems Inc
- Quantity
- 190 units (38 - 5 pack shelf cartons)
- Distribution
- US Nationwide distribution.
- Recall date
- July 6, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)