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LeMaitre Vascular Recalls

70 recalls on record · April 10, 2013 to March 25, 2026 · Medical Devices

Recalls by year

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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.

August 3, 2016Medical DevicesFDA
LeMaitre Vascular, Inc. recalls AnastoCiip Universal Clip Remover (1Each} REF# e4001-04 The Anastoclip Clip applier consists of a rotating shaft and
Hazard: US marketing brochure for the AnastoClip AC Closure System states that the Anastoclip catalog numbers can be used for dura closure, but the catalog numbers are only intended for cardiovascular use.
August 3, 2016Medical DevicesFDA
LeMaitre Vascular, Inc. recalls AnastoCiip Universal Clip Remover (6 Pack} REF# e4001-00 The Anastoclip Clip applier consists of a rotating shaft a
Hazard: US marketing brochure for the AnastoClip AC Closure System states that the Anastoclip catalog numbers can be used for dura closure, but the catalog numbers are only intended for cardiovascular use.
August 3, 2016Medical DevicesFDA
LeMaitre Vascular, Inc. recalls AnastoCiip Universal Clip Remover (1Each} REF# 4001-04 The Anastoclip Clip applier consists of a rotating shaft and
Hazard: US marketing brochure for the AnastoClip AC Closure System states that the Anastoclip catalog numbers can be used for dura closure, but the catalog numbers are only intended for cardiovascular use.
August 3, 2016Medical DevicesFDA
LeMaitre Vascular, Inc. recalls AnastoCiip Universal Clip Remover (6 Pack} REF# 4001-00 The Anastoclip Clip applier consists of a rotating shaft a
Hazard: US marketing brochure for the AnastoClip AC Closure System states that the Anastoclip catalog numbers can be used for dura closure, but the catalog numbers are only intended for cardiovascular use.
August 3, 2016Medical DevicesFDA
LeMaitre Vascular, Inc. recalls Anasto AC Closure System and Anasto Universal Clip Remover- Anasto AC 8cm 25 Clips (1 Each} X-Large REF # 4000-08
Hazard: US marketing brochure for the AnastoClip AC Closure System states that the Anastoclip catalog numbers can be used for dura closure, but the catalog numbers are only intended for cardiovascular use.
August 3, 2016Medical DevicesFDA
LeMaitre Vascular, Inc. recalls AnastoClip AC 8cm 35 Clips (1 Each} Large REF # 4000-07 The Anastoclip Clip applier consists of a rotating shaft an
Hazard: US marketing brochure for the AnastoClip AC Closure System states that the Anastoclip catalog numbers can be used for dura closure, but the catalog numbers are only intended for cardiovascular use.
August 3, 2016Medical DevicesFDA
LeMaitre Vascular, Inc. recalls Anastoclip AC 8cm 35 Clips (1 Each} Medium REF # 4000-06 The Anastoclip Clip applier consists of a rotating shaft an
Hazard: US marketing brochure for the AnastoClip AC Closure System states that the Anastoclip catalog numbers can be used for dura closure, but the catalog numbers are only intended for cardiovascular use
December 16, 2015Medical DevicesFDA
LeMaitre Vascular, Inc. recalls LeMaitre NovaSil Silicone Single Lumen Embolectomy Catheter 2F, 60 cm, Model e1801-26. Indicated for the removal of art
Hazard: Manufacturing issue that could cause a pinhole in the formed end of the packaging, which may lead to compromised sterility.
December 16, 2015Medical DevicesFDA
LeMaitre Vascular, Inc. recalls LeMaitre NovaSil Silicone Single Lumen Embolectomy Catheter 6F, 80 cm, Model 1601-68. Indicated for the removal of arte
Hazard: Manufacturing issue that could cause a pinhole in the formed end of the packaging, which may lead to compromised sterility.
December 16, 2015Medical DevicesFDA
LeMaitre Vascular, Inc. recalls LeMaitre Single Lumen Embolectomy Catheter 5F, 80 cm, Model 1601-58 and e1601-58. Indicated for the removal of arterial
Hazard: Manufacturing issue that could cause a pinhole in the formed end of the packaging, which may lead to compromised sterility.
December 16, 2015Medical DevicesFDA
LeMaitre Vascular, Inc. recalls LeMaitre Single Lumen Embolectomy Catheter 4F, 80 cm, Model 1601-48 and e1601-48. Indicated for the removal of arterial
Hazard: Manufacturing issue that could cause a pinhole in the formed end of the packaging, which may lead to compromised sterility.
December 16, 2015Medical DevicesFDA
LeMaitre Vascular, Inc. recalls LeMaitre Single Lumen Embolectomy Catheter 3F, 80 cm, Model 1601-38 and e1601-38. Indicated for the removal of arterial
Hazard: Manufacturing issue that could cause a pinhole in the formed end of the packaging, which may lead to compromised sterility.
December 16, 2015Medical DevicesFDA
LeMaitre Vascular, Inc. recalls LeMaitre Over-the-Wire Embolectomy Catheter 6F, 80 cm, Model e-1651-68. Indicated for the removal of arterial emboli
Hazard: Manufacturing issue that could cause a pinhole in the formed end of the packaging, which may lead to compromised sterility.
December 16, 2015Medical DevicesFDA
LeMaitre Vascular, Inc. recalls LeMaitre Over-the-Wire Embolectomy Catheter 6F, 40 cm, Model e-1651-64. Indicated for the removal of arterial emboli an
Hazard: Manufacturing issue that could cause a pinhole in the formed end of the packaging, which may lead to compromised sterility.
December 16, 2015Medical DevicesFDA
LeMaitre Vascular, Inc. recalls LeMaitre Over-the-Wire Embolectomy Catheter 5F Plus, 40 cm, Model e1651-84. Indicated for the removal of arterial embol
Hazard: Manufacturing issue that could cause a pinhole in the formed end of the packaging, which may lead to compromised sterility.
December 16, 2015Medical DevicesFDA
LeMaitre Vascular, Inc. recalls LeMaitre Over-the-Wire Embolectomy Catheter 7F, 80cm, Model 1654-78 and e1654-78. Indicated for the removal of arterial
Hazard: Manufacturing issue that could cause a pinhole in the formed end of the packaging, which may lead to compromised sterility.
December 16, 2015Medical DevicesFDA
LeMaitre Vascular, Inc. recalls LeMaitre Over-the-Wire Embolectomy Catheter 5F Plus, 80cm, Model 1651-88 and e1654-88. Indicated for the removal of art
Hazard: Manufacturing issue that could cause a pinhole in the formed end of the packaging, which may lead to compromised sterility.
December 16, 2015Medical DevicesFDA
LeMaitre Vascular, Inc. recalls LeMaitre Over-the-Wire Embolectomy Catheter 4F, 80cm, Model 1651-48 and e1654-48. Indicated for the removal of arterial
Hazard: Manufacturing issue that could cause a pinhole in the formed end of the packaging, which may lead to compromised sterility.
December 16, 2015Medical DevicesFDA
LeMaitre Vascular, Inc. recalls LeMaitre Over-the-Wire Embolectomy Catheter 3F, 80cm, Model 1651-38. Indicated for the removal of arterial emboli and t
Hazard: Manufacturing issue that could cause a pinhole in the formed end of the packaging, which may lead to compromised sterility.
December 16, 2015Medical DevicesFDA
LeMaitre Vascular, Inc. recalls LeMaitre Over-the-Wire Embolectomy Catheter 3F, 40cm, Model 1651-34 and e1651-34. Indicated for the removal of arterial
Hazard: Manufacturing issue that could cause a pinhole in the formed end of the packaging, which may lead to compromised sterility.
March 25, 2015Medical DevicesFDA
LeMaitre Vascular, Inc. recalls LeMaitre Vascular Tumescent Catheter Inversion (TCI) System. The TCI System is intended to provide a system to the re
Hazard: Mislabeled with an incorrect expiration date
July 31, 2013Medical DevicesFDA
LeMaitre Vascular, Inc. recalls AlboGraft Woven with Collagen, Straight 30x26 Catalog Number: ATC3026 AlboGraft Vascular Grafts are made of syntheti
Hazard: Blood blushing/leaking from the surface of the graft after implantation
July 31, 2013Medical DevicesFDA
LeMaitre Vascular, Inc. recalls AlboGraft Woven with Collagen, Straight 30x24 Catalog Number: ATC3024 AlboGraft Vascular Grafts are made of syntheti
Hazard: Blood blushing/leaking from the surface of the graft after implantation
July 31, 2013Medical DevicesFDA
LeMaitre Vascular, Inc. recalls AlboGraft Woven with Collagen, Straight 30x18 Catalog Number: ATC3018 AlboGraft Vascular Grafts are made of syntheti
Hazard: Blood blushing/leaking from the surface of the graft after implantation
July 31, 2013Medical DevicesFDA
LeMaitre Vascular, Inc. recalls AlboGraft Woven with Collagen, Straight 30x16 Catalog Number: ATC3016 AlboGraft Vascular Grafts are made of syntheti
Hazard: Blood blushing/leaking from the surface of the graft after implantation
July 31, 2013Medical DevicesFDA
LeMaitre Vascular, Inc. recalls AlboGraft Woven with Collagen, Straight 15x30 Catalog Number: ATC1530 AlboGraft Vascular Grafts are made of synthetic
Hazard: Blood blushing/leaking from the surface of the graft after implantation
July 31, 2013Medical DevicesFDA
LeMaitre Vascular, Inc. recalls AlboGraft Woven with Collagen, Straight 15x26 Catalog Number: ATC1526 AlboGraft Vascular Grafts are made of syntheti
Hazard: Blood blushing/leaking from the surface of the graft after implantation
July 31, 2013Medical DevicesFDA
LeMaitre Vascular, Inc. recalls AlboGraft Knitted with Collagen, Straight 60x08 Catalog Number: AMC6008 AlboGraft Vascular Grafts are made of synthe
Hazard: Blood blushing/leaking from the surface of the graft after implantation
July 31, 2013Medical DevicesFDA
LeMaitre Vascular, Inc. recalls AlboGraft Knitted with Collagen, Straight 60x07 Catalog Number: AMC6007 AlboGraft Vascular Grafts are made of synthe
Hazard: Blood blushing/leaking from the surface of the graft after implantation
July 31, 2013Medical DevicesFDA
LeMaitre Vascular, Inc. recalls AlboGraft Knitted with Collagen, Straight 60x06 Catalog Number: AMC6006 AlboGraft Vascular Grafts are made of synthe
Hazard: Blood blushing/leaking from the surface of the graft after implantation