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FDA (Device enforcement)Recalled 2018-01-03closedclass ii

Medtronic Perfusion Systems: Medtronic Custom Perfusion Systems, indicated for use in the extracorporeal circuit during cardiopulmonary bypass (CPB) surgical procedures.

Is my product affected?

Medtronic Custom Perfusion Systems, indicated for use in the extracorporeal circuit during cardiopulmonary bypass (CPB) surgical procedures.

  • UPC 20885074191038
  • UPC 00613994268174
  • UPC 20643169876648
  • UPC 00643169845121
  • UPC 00763000025878
  • UPC 00643169845077
  • UPC 00643169872127
  • UPC 00643169741591
  • UPC 00643169735989
  • UPC 00643169906181
  • UPC 20613994490760
  • UPC 00643169471986
  • UPC 00643169789517
  • UPC 00643169510432
  • UPC 00643169661295
  • UPC 00643169715097

Check against the official notice below — it lists the full affected range.

What happened

Medtronic custom perfusion tubing packs used during heart-lung bypass surgery have been recalled because they contain Terumo OPS valves that may not allow proper fluid flow through the valve. A total of 2,914 units with various reference numbers and lot serial numbers were distributed to Delaware, Iowa, California, and Japan.

The recall record does not specify what remedy is available to affected consumers.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Medtronic custom perfusion tubing packs contain Terumo OPS valves that were recalled due to a lack of flow through the valve.

Details from the source

Reason for recall: Medtronic custom perfusion tubing packs contain Terumo OPS valves that were recalled due to a lack of flow through the valve. Distribution: DE, IA, CA and Japan Quantity: 2914 units Lot/code info: a) REF 2815R1, UPN/GTIN: 20885074191038, Lot/Serial Numbers: 210937492, 213151103, 213671744 b) REF 2D25R6, UPN/GTIN: 00613994268174, Lot/Serial Numbers: 209533592, 209759280, 209948919, 210174899, 210377603, 210478517, 210591995, 210767149, 211011818, 211210404, 211243436, 211542842, 211761616 c) REF 9M68R, UPN/GTIN: 20643169876648, Lot/Serial Numbers: 212067087, 212796361 d) REF BB4B15R13, UPN/GTIN: 00643169845121, Lot/Serial Numbers: 211804184, 212073924, 212266962, 212268301, 212385983, 212552883, 212796215, 213248430, 213583108 e) REF BB4B15R14, UPN/GTIN: 00763000025878, Lot/Serial Numbers: 213801240, 213868837 f) REF BB9L72R, UPN/GTIN: 00643169845077, Lot/Serial Numbers: 211715103 g) REF BB9L72R1, UPN/GTIN: 00643169872127, Lot/Serial Numbers: 212020797, 212174623, 212193001, 212301586, 212355584, 212428238, 212626142, 212884370, 213001157, 213248459, 213631247, 213672934, 213802501, 214072742, 214093025 h) REF CB1Z87R11, UPN/GTIN: 00643169741591, Lot/Serial Numbers: 211755326 i) REF CB4L56R24, UPN/GTIN: 00643169735989, Lot/Serial Numbers: 211654744, 211654745, 211800954 j) REF CB4L56R26, UPN/GTIN: 00643169906181, Lot/Serial Numbers: 212294432, 212404544, 212447345, 212489670, 213251146, 213251166, 213358174, 213573495, 213623995, 214053395 k) REF CB5S68R3, UPN/GTIN: 20613994490760, Lot/Serial Numbers: 210937507 l) REF CB7X82R4, UPN/GTIN: 00643169471986, Lot/Serial Numbers: 211050766, 211320749 m) REF CB7X82R5, UPN/GTIN: 00643169789517, Lot/Serial Numbers: 211423503, 211

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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