Route 92 Medical 070 Reperfusion System recall
Route 92 Medical 070 Reperfusion System, REF 1003, Rxonly, SterileEO. Used for introduction of interventional devices into the neurovasculature and…
Why was Route 92 Medical 070 Reperfusion System recalled?
Their is the potential for distal tip separation at the proximal marker band of the delivery catheters
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
UDI: 00853799007169/ Lot # 23112702 and 23112901
- Product
- Route 92 Medical 070 Reperfusion System, REF 1003, Rxonly, SterileEO. Used for introduction of interventional devices into the neurovasculature and…
- Recalling firm
- ROUTE 92 MEDICAL INC
- Quantity
- 19 units
- Distribution
- US: AL AZ CA DE FL GA IA IL IN KY LA MA MD MI MN MO NC ND NJ NY OH OR PA RI SD TN TX UT VA WV OUS: New Zealand
- Recall date
- May 1, 2024
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)