Home / Brands / Smith & Nephew, Inc. Endoscopy Division
Smith & Nephew, Inc. Endoscopy Division Recalls
37 recalls on record · August 15, 2012 to July 23, 2014 · Medical Devices
Recalls by year
12
13
14
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 23, 2014Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls SUTUREFIX Ultra S Double Loaded Suture Product Code: 72203854 Fastener, fixation, nondegradable, soft tissue
Hazard: Sterility of device is compromised due to breach in sterile barrier
July 23, 2014Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls SUTUREFIX Ultra S with 1 #2 Ultrabraid Suture (blue/white) Product Code: 72203853 Fastener, fixation, nondegradable,
Hazard: Sterility of device is compromised due to breach in sterile barrier
July 23, 2014Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls SUTUREFIX Ultra S with 1 #2 Ultrabraid (blue) Product Code: 72203852 Fastener, fixation, nondegradable, soft tissue
Hazard: Sterility of device is compromised due to breach in sterile barrier
July 23, 2014Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Cobraid Suture Product Code: 72203842 Fastener, fixation, nondegr
Hazard: Sterility of device is compromised due to breach in sterile barrier
July 23, 2014Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Blue Product Code: 72203841 Fastener, fixation, nondegradable,
Hazard: Sterility of device is compromised due to breach in sterile barrier
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls TWINFIX Ultra 6.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures (blue, blue-COBRAID) with Needles; Part Number
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls TWINFIX Ultra 5.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures (blue, blue-COBRAID) with Needles; Part Number
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls TWINFIX" Ultra 4.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures (blue, blue-COBRAID") with Needles; Part Numb
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls RAPTORMITE" 3.7 mm PLLA with two ULTRABRAID" Sutures Size 0 and Needles; Part Number: 72201805 Biodegradable suture a
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls TWINFIX Ultra PLLA/HA 6.5 mm with 3 ULTRABRAID Suture; Part Number: 72202610 Biodegradable suture anchor
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls TWINFIX" Ultra PLLA/HA 6.5 mm with 2 ULTRABRAID" Suture, White / Black: Part Number: 72202608 Biodegradable suture an
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls TWINFIX ULTRA PLLA/HA 5.5 mm Suture Anchor with 3 ULTRABRAID Suture: Part Number: 72202603 Biodegradable suture ancho
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls TWINFIX Ultra PLLA/HA 5.5 mm Suture Anchor with 2 ULTRABRAID Suture, White / Black: Part Number: 72202602 Biodegradab
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls TWINFIX Ultra HA 6.5 mm with 2 ULTRABRAID Suture, Blue / Black; Part Number: 72202631 Biodegradable suture anchor
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls TWINFIX Ultra HA 5.5 mm Suture Anchor with 2 ULTRABRAID Suture, Blue / Black; Part Number: 72202626 Biodegradable su
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture, Blue / Black; Part Number: 72202624 Biodegradable su
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture, White / Blue; Part Number: 72202597 Biodegradable su
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls OSTEORAPTOR CURVED 2.3 mm Suture Anchor SA ULTRABRAID COBRAID Suture, Blue; Part Number: 72203290 Biodegradable sutu
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls OSTEORAPTOR CURVED 2.3 mm Suture Anchor ULTRABRAID COBRAID Suture, Black; Part Number: 72203291 Biodegradable suture
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls OSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID Suture, White; Part Number: 72202165 Biodegradable suture anchor
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture, White / Black; Part Number: 72201996 Biodegradable suture
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls OSTOSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture, Blue; Part Number: 72201994 Biodegradable sutu
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls OSTEORAPTOR 2.3 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture, Black; Part Number: 72201992 Biodegradable suture
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls OSTEORAPTOR 2.3 mm with 1 ULTRABRAID Suture, White; Part Number: 72201991 Biodegradable suture anchor
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture, White / Blue ; Part Number: 72201995 Biodegradable suture
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls OSTEORAPTOR 2.3 mm Suture Anchor with ULTRABRAID COBRAID Suture, Blue; Part Number: 72201993 Biodegradable suture a
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls BIORAPTOR 2.9 mm Suture Anchor, pack of 1 ULTRABRAID Suture: 72200689 Biodegradable suture anchor
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls BIORAPTOR 2.9 mm Suture Anchor Straight, pack of 2 ULTRABRAID Suture; Part Number: 72200690 Biodegradable suture anch
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls BIORAPTOR 2.9 mm Suture Anchor with DURABRAID" Suture; Part Number: 72200783 Biodegradable suture anchor
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls BIORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID Suture; Part Number: 72200774 Biodegradable suture anchor
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.