FDA Recall Terminated

Peripheral Diamondback 1.50 Solid OAD, a percutaneous orbital atherectomy system indicated for use as therapy in patients with occlusive atherosclerotic disease in peripheral arteries and who are acceptable candidates for percutaneous transluminal atherectomy.

Recall: Z-0506-2018 · Initiated September 14, 2017

Recall

Recall Number
Z-0506-2018
Event Number
78897
Firm
Cardiovascular Systems Inc
FEI Number
3004742232
Product Code
MCW
Status
Terminated
Root Cause
Labeling mix-ups
Initiated
September 14, 2017
Terminated
November 4, 2019
Address
1225 Old Highway 8 NW, Saint Paul, MN, 55112-6416

Description

Peripheral Diamondback 1.50 Solid OAD, a percutaneous orbital atherectomy system indicated for use as therapy in patients with occlusive atherosclerotic disease in peripheral arteries and who are acceptable candidates for percutaneous transluminal atherectomy.

Reason

Cardiovascular Systems, Inc. (CSI) is removing the products because it was identified that the labeling for two lots of product s were potentially inadvertently switched during production.

Action

On 09/14/2017 the firm sent letters to their consignees explaining the recall and given the following instructions: Please immediately remove from use and return the affected Product Name devices to CSI. To do so: 1) Complete the attached Customer Acknowledgement Form a. Per lot, document the quantity of all devices that are to be returned. b. Per lot, document the quantity of all devices that have been consumed. 2) Place the Acknowledgement Form with the device 3) Return the device and Acknowledgement Form to CSI using the pre-paid FedEx label a. If you would like, a CSI Sales Representative can return the device and form. Please contact the CSI Recall Coordinator to organize pick up and return of the product. If all products specified in this recall notice have previously been consumed, used or are no longer available for return to CSI, please complete the Customer Acknowledgment Form per the above, and return the form to CSI in the provided FedEx envelope. Contact Information: [email protected] 651-259-2800 - Tel

Distribution

FL, IL, MI, MN, MO, NY, SC, TX, and WI

Quantity

8