DIAMONDBACK 360 Peripheral 1.50 Classic recall
DIAMONDBACK 360 Peripheral 1.50 Classic, Model DBP-150CLASS145 Peripheral Orbital Atherectomy System (OAS) is a minimally invasive, catheter-based OAS…
Why was DIAMONDBACK 360 Peripheral 1.50 Classic recalled?
CSI discovered that a 1.50mm Solid Crown OAD was labeled as a 1.50mm Crown OED.
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: 171686, Expiration: 2018-09-30
- Product
- DIAMONDBACK 360 Peripheral 1.50 Classic, Model DBP-150CLASS145 Peripheral Orbital Atherectomy System (OAS) is a minimally invasive, catheter-based OAS…
- Recalling firm
- Cardiovascular Systems Inc
- Quantity
- 8 units
- Distribution
- Nationwide Distribution to LA, MS, SC, TX
- Recall date
- March 1, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)