Medtronic Perfusion Systems

95 recalls • • Categories: Infusion Pumps, Other Medical Devices, Surgical Instruments, Diagnostic Equipment

As of August 6, 2025, Medtronic has received eleven reports of VitalFlow Consoles displaying an E70 error code during normal operation. When this occurs, the touch screen may become temporarily unresponsive and go blank for up to two minutes before recovering to full functionality. Importantly, the console continues to maintain set pump speed and function throughout.

Oct 3, 2025 Infusion Pumps Nationwide View Details →

Unexpected loose material in the male luer used in the aortic root cannula has been identified. Potential harms when identified prior to use - procedure delay. Potential harm if not identified and used - stroke (reversible and irreversible).

Feb 5, 2025 Other Medical Devices Nationwide View Details →

Potential for unsealed sterile packing.

Mar 19, 2024 Surgical Instruments View Details →

Potential for unsealed sterile packing.

Mar 19, 2024 Diagnostic Equipment View Details →

Potential for unsealed sterile packing.

Mar 19, 2024 Other Medical Devices View Details →

Medtronic Arterial Cannulae packaged as: a) DLPÂż Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80020; b) DLPÂż Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80220; c) DLPÂż Curved Metal Tip Arterial Cannula 20 Fr., Model Number 82020; d) DLPÂż Curved Metal Tip Arterial Cannula 20 Fr., Model Number 87120; e) DLPÂż Curved Metal Tip Arterial Cannula 22 Fr. , Model Number 80222; f) DLPÂż Curved Metal Tip Arterial Cannula 22 Fr. , Model Number 87122; g) DLPÂż Curved Tip Arterial Cannula 20 Fr., Model Number 87220; h) DLPÂż Curved Tip Arterial Cannula 22 Fr., Model Number 87222; i) DLP" One-Piece Arterial Cannulae, Pediatric 6 Fr, Model Number 77006; j) DLP" One-Piece Pediatric Arterial Cannula 6 Fr, Model Number 77206; k) DLP" One-Piece Pediatric Arterial Cannula 8 Fr, Model Number 77008; l) DLP" One-Piece Pediatric Arterial Cannula 10 Fr, Model Number 77010; m) DLP" One-Piece Pediatric Arterial Cannula 10 Fr, Model Number 77110; n) DLP" One-Piece Pediatric Arterial Cannula 12 Fr, Model Number 77112; o) EOPA" Elongated One Piece Arterial Cannula 20 Fr., Model Number 77420; p) EOPA" Elongated One Piece Arterial Cannula 22 Fr., Model Number 77422; q) EOPA" Elongated One Piece Arterial Cannula 22 Fr., Model Number 77522; r) EOPA" Elongated One Piece Arterial Cannula 22 Fr., Model Number 77622; s) EOPA" Elongated One Piece Arterial Cannula 24 Fr., Model Number 77524; t) Select Series" Angled Tip Arterial Cannula 24Fr., Model Number 72424; u) Select Series" Straight Tip Arterial Cannula 20 Fr., Model Number 72120; v) Select Series" Straight Tip Arterial Cannula 24 Fr., Model Number 72224

Class I - Dangerous

Potential for unsealed sterile packing.

Mar 19, 2024 Other Medical Devices View Details →

Medtronic Venous Cannulae: a) DLPÂż 20 Fr. Malleable Single Stage Venous Cannula, Model Number 68120, b) DLPÂż 24 Fr. Malleable Single Stage Venous Cannula, Model Number 68124, c) DLPÂż 28 Fr. Malleable Single Stage Venous Cannula, Model Number 68128, d) DLPÂż 30 Fr. Malleable Single Stage Venous Cannula, Model Number 68130, e) DLPÂż 34 Fr. Malleable Single Stage Venous Cannula, Model Number 68134, f) DLPÂż 12 Fr. Single Stage Venous Cannula, Model Number 67312, g) DLPÂż 16 Fr. Single Stage Venous Cannula, Model Number 67316, h) DLPÂż 16 Fr. Single Stage Venous Cannula, Model Number 67516, i) DLPÂż 18 Fr. Single Stage Venous Cannula, Model Number 66118, j) DLPÂż 18 Fr. Single Stage Venous Cannula, Model Number 67318, k) DLPÂż 20 Fr. Single Stage Venous Cannula, Model Number 67320, l) DLPÂż 20 Fr. Single Stage Venous Cannula, Model Number 69320, m) DLPÂż 20 Fr. Single Stage Venous Cannula, Model Number 67520, n) DLPÂż 22 Fr. Single Stage Venous Cannula, Model Number 66122, o) DLPÂż 22 Fr. Single Stage Venous Cannula, Model Number 67522, p) DLPÂż 24 Fr. Single Stage Venous Cannula, Model Number 67524, q) DLPÂż 26 Fr. Single Stage Venous Cannula, Model Number 67526, r) DLPÂż 28 Fr. Single Stage Venous Cannula, Model Number 66128, s) DLPÂż 28 Fr. Single Stage Venous Cannula, Model Number 39628, t) DLPÂż 28 Fr. Single Stage Venous Cannula, Model Number 67528, u) DLPÂż 30 Fr. Single Stage Venous Cannula, Model Number 66130, v) DLPÂż 31 Fr. Single Stage Venous Cannula, Model Number 69331, w) DLPÂż 32 Fr. Single Stage Venous Cannula, Model Number 66132, x) DLPÂż 34 Fr. Single Stage Venous Cannula, Model Number 67534, y) DLPÂż 36 Fr. Single Stage Venous Cannula, Model Number 66236, z) MC2Âż 28/36 Fr. Two Stage Venous Cannula, Model Number 91228, aa) MC2Âż 29/37 Fr. Two Stage Venous Cannula, Model Number 91229C, bb) MC2Âż 32/40 Fr. Two Stage Venous Cannula, Model Number 91263, cc) MC2Âż 32/40 Fr. Two Stage Venous Cannula, Model Number 91240C, dd) MC2Âż 32/40 Fr. Two Stage Venous Cannula, Model Number 91263C, ee) MC2Âż 34/46 Fr. Two Stage Venous Cannula, Model Number 91246, ff) MC2Âż 34/46 Fr. Two Stage Venous Cannula, Model Number 91246C, gg) MC2Âż 36/46 Fr. Two Stage Venous Cannula, Model Number 91236C, hh) MC2Âż 36/51 Fr. Two Stage Venous Cannula, Model Number 91251, ii) MC2Âż 36/51 Fr. Two Stage Venous Cannula, Model Number 91251C, jj) VC2" 34/38 Fr. Venous Cannula, Model Number 93438, kk) VC2" 34/48 Fr. Venous Cannula, Model Number 93448C

Class I - Dangerous

Potential for unsealed sterile packing.

Mar 19, 2024 Other Medical Devices View Details →

An upward trend of complaints in which the Temperature Monitoring Adapter (TMA), located on the Affinity Fusion Oxygenator, had come loose from the oxygenator either during pre-procedure perfusion set-up or post-procedure when disassembling the perfusion circuit.

Dec 12, 2022 Other Medical Devices Nationwide View Details →

An upward trend of complaints in which the Temperature Monitoring Adapter (TMA), located on the Affinity Fusion Oxygenator, had come loose from the oxygenator either during pre-procedure perfusion set-up or post-procedure when disassembling the perfusion circuit.

Dec 12, 2022 Other Medical Devices Nationwide View Details →

An upward trend of complaints in which the Temperature Monitoring Adapter (TMA), located on the Affinity Fusion Oxygenator, had come loose from the oxygenator either during pre-procedure perfusion set-up or post-procedure when disassembling the perfusion circuit.

Dec 12, 2022 Other Medical Devices Nationwide View Details →

Medtronic Custom Perfusion kits, with the following product descriptions and corresponding model numbers: 1. CUSTOM PACK BB10Q85R FILTER (Model BB10Q85R); 2. CUSTOM PACK BB11C01R MIDI DEEP (Model BB11C01R); 3. CUSTOM PACK BB7H95R22 HYP MAIN (Model B7H95R22); 4. CUSTOM PACK BB7H95R25 HYP MAIN (Model BB7H95R25); 5. CUSTOM PACK BB7H99R22 NEONAT (Model BB7H99R22); 6. CUSTOM PACK BB7P46R4 316-14 (Model BB7P46R4); 7. CUSTOM PACK BB7P48R4 14-38 (Model BB7P48R4); 8. CUSTOM PACK BB7W03R8 CCSM NEON (Model BB7W03R8); 9. CUSTOM PACK BB7W80R7 BASC PEDS (Model BB7W80R7); 10. CUSTOM PACK BB8B09R7 INFANT (Model BB8B09R7); 11. CUSTOM PACK BB8B09R8 INFANT (Model BB8B09R8); 12. CUSTOM PACK BB8D40R3 P3/16X1/4 (Model BB8D40R3); 13. CUSTOM PACK BB8Q16R PED ART (Model BB8Q16R); 14. CUSTOM PACK BB8V01R8 FVDL COLM (Model BB8V01R8); 15. CUSTOM PACK HY2V10R33 ADULT (Model HY2V10R33); 16. CUSTOM PACK HY3Z71R17 PRIMARY (Model HY3Z71R17); 17. CUSTOM PACK HY3Z71R18 PRIMARY (Model HY3Z71R18); 18. CUSTOM PACK HY4V00R24 ADULT (Model HY4V00R24); 19. CUSTOM PACK HY6X29R12 CON-SUPP (Model HY6X29R12); 20. CUSTOM PACK HY8L14R7 HYBRID (Model HY8L14R7); 21. CUSTOM PACK HY8P36R6 CPS (Model HY8P36R6); 22. CUSTOM PACK HY8V01R6 FVDL COLM (Model HY8V01R6); 23. CUSTOM PACK HY9D36R1 HL PUMP P (Model HY9D36R1); 24. CUSTOM PACK HY9L07R4 ADLT FUS (Model HY9L07R4); 25. CUSTOM PACK HY9L80R4 SADT FUS (Model HY9L80R4); 26. CUSTOM PACK HY9M47R6 ADLT MAIN (Model HY9M47R6); 27. CUSTOM PACK HY9N38R4 VGH FUS (Model HY9N38R4); 28. CUSTOM PACK HY9R26R12 CENT (Model HY9R26R12); 29. PERFUSION M337112Q 1/B (Model M337112Q); 30. PERFUSION M344130B 1/B (Model M344130B); 31. PERFUSION M392419C 1/B (Model M392419C); 32. PERFUSION M394213B 1/B (Model M394213B); 33. PERFUSION M394213C 1/B (Model M394213C); 34. PERFUSION M490124D 1/B (Model M490124D); 35. PERFUSION M491335A 1/B (Model M491335A); 36. PERFUSION M499709E 1/B (Model M499709E); 37. PERFUSION M960164F 1/B (Model M960164F); 38. PERFUSION M960165E 1/B (Model M960165E); 39. PERFUSION M960169E 1/B (Model M960169E); 40. PERFUSION M960462C 1/B (Model M960462C); 41. PERFUSION M960462D 1/B (Model M960462D); 42. PERFUSION M960463D 1/B (Model M960463D); 43. PERFUSION M960466D 1/B (Model M960466D); 44. CUSTOM PACK TL4K33R3 FCI ADULT (Model TL4K33R3); 45. CUSTOM PACK TL4K95R12 PERFNPLEG (Model TL4K95R12); 46. CUSTOM PACK TL6C91R5 SELLKE PK (Model TL6C91R5); 47. CUSTOM PACK TL6G48R9 ST PAULS (Model TL6G48R9); 48. CUSTOM PACK TL7X09R3 FCVC ADLT (Model TL7X09R3);

Class I - Dangerous

Product is labeled as non-pyrogenic but endotoxin testing was not performed.

Oct 12, 2021 Infusion Pumps Nationwide View Details →

An electrical component within the system controller module of certain Bio-Console 560 devices may exhibit electrical failure causing the device to stop pumping. Issues observed include the pump stopping, the user interface going blank, and smoking and producing a burning odor during use.

Mar 3, 2021 Infusion Pumps Nationwide View Details →

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

Feb 4, 2021 Infusion Pumps Nationwide View Details →

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

Feb 4, 2021 Infusion Pumps Nationwide View Details →

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

Feb 4, 2021 Infusion Pumps Nationwide View Details →

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

Feb 4, 2021 Infusion Pumps Nationwide View Details →

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

Feb 4, 2021 Infusion Pumps Nationwide View Details →

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

Feb 4, 2021 Infusion Pumps Nationwide View Details →

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

Feb 4, 2021 Infusion Pumps Nationwide View Details →

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

Feb 4, 2021 Infusion Pumps Nationwide View Details →

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

Feb 4, 2021 Infusion Pumps Nationwide View Details →

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

Feb 4, 2021 Infusion Pumps Nationwide View Details →

Medtronic discovered that certain Y-connectors included in the suction lines have exhibited tearing and cracking. These defects could cause the Y-connectors to leak when in use, which could result in potential blood loss and a breach in the circuit.

Nov 27, 2018 Other Medical Devices Nationwide View Details →

Medtronic discovered that certain Y-connectors included in the suction lines have exhibited tearing and cracking. These defects could cause the Y-connectors to leak when in use, which could result in potential blood loss and a breach in the circuit.

Nov 27, 2018 Other Medical Devices Nationwide View Details →

Medtronic has been unable to develop a cleaning protocol to satisfy current industry concerns and expectations. As a result, an updated cleaning protocol will not be developed by Medtronic and it has been determined that the best course of action is to request BIO CAL users to discontinue use and dispose of BIO CAL devices.

Feb 8, 2018 Other Medical Devices View Details →

Possible sterile barrier breach in the pouch of Affinity NT Cardiotomy Venous Reservoir stand alone uncoated and Affinity NT Cardiotomy Venous Reservoir stand alone Trillium coated products.

Jan 16, 2018 Other Medical Devices View Details →

Possible sterile barrier breach in the pouch of Affinity NT Cardiotomy Venous Reservoir stand alone uncoated and Affinity NT Cardiotomy Venous Reservoir stand alone Trillium coated products.

Jan 16, 2018 Other Medical Devices View Details →

Identification of small pinholes in a single packaging configuration of sterile pouches. A total of seven different products were affected.

Jun 22, 2017 Diagnostic Equipment Nationwide View Details →

Medtronic is notifying customers who have or may receive specific lots of Medtronic Perfusion Tubing Packs that include the potentially affected cuvettes manufactured by Terumo Cardiovascular Systems (Terumo CVS). Terumo Cardiovascular Systems (Terumo CVS) has distributed an Urgent Safety Alert regarding the CD IÂż H/S Cuvette. The cuvette is packaged into Medtronic Perfusion Tubing Packs and only sold as part of the pack.

Feb 4, 2016 Other Medical Devices Nationwide View Details →

This recall is being initiated due to a potential breach of the Tubing Pack Header Bags manufactured in these select lots. The seal in question is between the Tyvek and the Poly side of the header bag.

Oct 28, 2015 Infusion Pumps Nationwide View Details →

Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration performance that is below product specification. These potentially affected units have been distributed as stand-alone devices and in specific lots of Medtronic Perfusion Tubing packs.

Aug 18, 2015 Other Medical Devices Nationwide View Details →

Medtronic is recalling select lots of DLP Femoral Arterial Cannula product due to recent reports in which the user had difficulty or was unable to connect the cannula to the perfusion circuit tubing.

Jun 12, 2015 Diagnostic Equipment View Details →

Medtronic initiated an Urgent Medical Device Recall for 66 distributed Affinity FusionTM Oxygenation Systems with Carmeda Bioactive Surface due to damaged heat exchangers. Product affected by this issue is limited to model CB841 sold stand alone or incorporated in Total Systems TS1614R1 and TS1595R7. UPDATED: Recall was updated to incorporate three additional lots affected.

Oct 31, 2014 Infusion Pumps View Details →