Medtronic Recalls Sherpa NX Active Guiding Catheters Due to Material Loss
Medtronic Vascular is recalling 9 units of Sherpa NX Active Guiding Catheters because primary segment material may be lost, exposing underlying stainless-steel braid wires.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a medical device with a structural defect that could expose sharp stainless-steel wires, posing a risk of harm to patients, but the source text does not report any specific injuries or illnesses.
Plain-English summary
Medtronic Vascular is recalling 9 units of the Sherpa NX Active Guiding Catheter, 6F SCR5.0, .070" (Reference SA6SCR50), for cardiovascular use. The recall was initiated because there is a potential for extensive loss of primary segment material on a subset of these catheters, which could expose the underlying stainless-steel braid wires.
The affected units were distributed worldwide to the United States, Austria, Belgium, Bulgaria, the Czech Republic, France, Germany, Greece, Hong Kong, Ireland, Italy, Kazakhstan, Luxembourg, Moldova, the Netherlands, Poland, Portugal, the Russian Federation, Saudi Arabia, Slovakia, South Africa, Spain, Sweden, Taiwan, and the United Kingdom. The recall covers all lot and serial numbers for the GTIN 00613994822567.
Healthcare providers and facilities should stop using the affected catheters and contact Medtronic Vascular for instructions on return or replacement. Patients who have had these catheters used during a procedure should consult their healthcare provider if they have concerns.
The recalled product
- Product
- SHERPA NX ACTIVE GUIDING CATHETER, 6F SCR5.0, .070", REF SA6SCR50. for cardiovascular use
- Manufacturer
- Medtronic Vascular
- Affected units
- 9
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- GTIN: 00613994822567 All Lot/Serial Numbers
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 191 recalled by Medtronic Vascular under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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