Every recall we track for Medtronic Vascular — 201 in all — plus the complaints and injury reports the public filed about them.
Medtronic Vascular recalls angiographic guidewire components with model numbers 107042, 107044, etc. due to improper sterilization process. Affected items may not be safe for medical use.
Medtronic recalls 6F Launcher Guide Catheter 100 cmJL 3.5 (LA6JL35) due to potential sterility compromise from an unsealed pouch. Affected units sold with lot code 220712186.
Medtronic recalls 6F Launcher Guide Catheter 100 cm JR 4.0 Model LA6JR40 with unsealed pouch risking sterility compromise. Affected units have specific lot codes.
Medtronic recalls 6F Launcher Guide Catheter 100cm EBU 3.75 (LA6EBU375) due to potential sterility compromise from an unsealed pouch. Affected units sold with specific lot codes.
Medtronic recalls 6F Launcher Guide Catheter 100 cm EBU 3.0 (LA6EBU30) due to potential sterility compromise from unsealed pouch. Affected units sold with lot code 220857555.
Medtronic Vascular recalls pediatric Rashkind Balloon Septostomy Catheters (5F, 50 cm) due to field failures and failed quality testing. Affected lot numbers include GFCT1699 through GFZ2173. Consumers should contact Medtronic for details.
a ~150-character meta description summarising the recall.
Medtronic Vascular recalls pediatric Rashkind Balloon Septostomy Catheters (6F, 50 cm) due to field failures and failed quality testing. Affected lot numbers include GFCP2154 through GFDZ1693. Consumers should contact Medtronic for details.
Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER models for potential wire exposure. Affected units may have stainless-steel braid wires exposed, risking injury during procedures.
Medtronic Vascular recalls specific SHERPA NX Active Guiding Catheters for possible exposure of stainless steel wires, posing a risk of injury during cardiovascular procedures.
Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER, 6F LCB SH, .070" REF SA6LCBSH for cardiovascular use due to potential loss of primary segment material exposing stainless-steel wires. Affected units may require replacement.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for possible wire exposure risk. Affected models include 6F MP ST, .070" with reference SA6MPST. Contact for remedy.
Medtronic Vascular recalls specific SHERPA NX Active Guiding Catheters due to potential loss of primary segment material exposing stainless steel wires. Affected units have a unique reference number and were sold for cardiovascular procedures.
Medtronic Vascular recalls SHERPA NX Active Guiding Catheters (6F JL4.5) due to potential wire exposure. Affected units may have stainless steel wires exposed, risking injury during procedures.
Medtronic Vascular recalls SHERPA NX 6F catheters due to potential wire exposure. Affected units may have stainless steel wires exposed, risking injury during procedures.
Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER models with potential wire exposure. Learn what to do if you own this device for cardiovascular procedures.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for potential wire exposure risk during cardiovascular procedures.
Medtronic recalls certain SHERPA NX Active Guiding Catheters for possible exposure of stainless steel wires, which could cause injury during cardiovascular procedures.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for potential wire exposure risk during cardiovascular procedures.
Medtronic Vascular recalls specific SHERPA NX Active Guiding Catheters for potential loss of primary segment material exposing stainless-steel wires. Affected units have model SA6ERADLSH and GTIN 00613994824738.
Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER models with potential for stainless-steel wire exposure. Affected units sold for cardiovascular procedures. Contact for return instructions.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for potential wire exposure risk during cardiovascular procedures. Affected models include 6F SAL3.0, .070" with reference SA6SAL30. No remedy details provided in recall notice.
Medtronic Vascular recalls specific SHERPA NX Active Guiding Catheters due to potential exposure of stainless steel wires. Affected units may cause injury during procedures. Contact for return instructions.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for potential wire exposure. Learn product details and safety steps.
a ~150-character meta description summarising the recall.
a ~150-character meta description summarising the recall.
Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER 6F models due to potential wire exposure. Affected units may have stainless steel wires exposed, risking injury during procedures.
Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER, 6F M RESS, .070" REF SA6MRESS for cardiovascular use due to potential loss of primary segment material exposing stainless-steel wires.
a ~150-character meta description summarising the recall.
Medtronic Vascular recalls SHERPA NX Active Guiding Catheters (6F JR3.5, .070", REF SA6JR35) due to potential loss of primary segment material exposing stainless-steel wires. This could cause complications during cardiovascular procedures.
a ~150-character meta description summarising the recall.
Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER, 6F RCB SH, .070" REF SA6RCBSH for cardiovascular use due to potential loss of primary segment material exposing stainless-steel wires.
Medtronic Vascular recalls specific SHERPA NX Active Guiding Catheters for possible wire exposure risk. Affected units may have stainless steel wires exposed, requiring immediate action.
a ~150-character meta description summarising the recall.
Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER models with potential for stainless-steel wire exposure. Affected units may require replacement.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for possible wire exposure risk. Affected units have a potential for stainless steel wires to become exposed, requiring immediate action.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for potential wire exposure risk during cardiovascular procedures.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for possible wire exposure risk during cardiovascular procedures.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for possible wire exposure risk during cardiovascular procedures.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for potential wire exposure risk during cardiovascular procedures. Affected units have a risk of stainless steel wires becoming exposed.
Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER models with potential wire exposure. Learn what to do if affected.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for potential loss of primary segment material exposing stainless steel wires. Affected units may require replacement to prevent injury during cardiovascular procedures.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for possible wire exposure risk during cardiovascular procedures.
Medtronic Vascular recalls specific SHERPA NX Active Guiding Catheters for potential wire exposure risk during cardiovascular procedures.
Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER model 6F MAC3.75 SH for potential wire exposure. Learn what to do if affected.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for possible wire exposure risk during cardiovascular procedures. Affected units include model 6F FR4.0, .070" with reference SA6FR40.
Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER models for potential wire exposure. Learn what to do if you own this device.
A ~150-character meta description summarising the recall.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for possible wire exposure risk during cardiovascular procedures.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for possible wire exposure risk during cardiovascular procedures. Affected units include 6F EBU4.0 models with serial number SA6EBU40.
Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER models with potential for wire exposure. Learn what to do if you own this device for cardiovascular procedures.
Medtronic Vascular recalls SHERPA NX Active Guiding Catheters (6F MAC3.5 SH) due to potential exposure of stainless steel wires. Affected units have specific model and serial numbers.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for possible wire exposure risk during cardiovascular procedures.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for potential wire exposure risk during cardiovascular procedures.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for potential wire exposure. Learn if your catheter is affected and what to do.
Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER 6F MB1 models due to potential loss of primary segment material exposing stainless-steel wires. Affected units may require medical evaluation.
Medtronic Vascular recalls SHERPA NX Active Guiding Catheters (6F AL2.0 SH) due to potential wire exposure. Affected units may have stainless steel wires exposed, risking injury during procedures.
Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER models with potential wire exposure. Learn what to do if you own this device for cardiovascular procedures.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for potential wire exposure during cardiovascular procedures. Affected models include 6F JR4.0, .070" with reference SA6JR405.
Medtronic recalls specific SHERPA NX Active Guiding Catheters for possible wire exposure. Affected units may have stainless steel wires exposed, risking injury during procedures.
