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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.
September 25, 2013Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls BIORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture; Part Number: 72200775 Biodegradable suture anchor
Hazard: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
August 15, 2012Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with three #2 sutures (white, COBRAID- blue), sterile Part Number: 722028
Hazard: Distal part of the anchor may break on insertion into bone during surgery
August 15, 2012Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures (COBRAID-blue, COBRAIDblack), sterile Part Number: 72
Hazard: Distal part of the anchor may break on insertion into bone during surgery
August 15, 2012Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures(white, COBRAID-blue), sterile Part Number: 72202895
Hazard: Distal part of the anchor may break on insertion into bone during surgery
August 15, 2012Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls Smith & Nephew 5.5 mm TWINFIX Ultra Ti Suture Anchor with two #2 ULTRABRAID sutures (blue, blue-COBRAID) with Needles
Hazard: Distal part of the anchor may break on insertion into bone during surgery
August 15, 2012Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls Smith & Nephew 5.5 mm Dyonics Bonecutter ,Electroblade Full Radius Part Number: 7205962 Product Usage: The Dyonic
Hazard: Device labeled with an expiry period of 48 months instead of 36 months; an additional 12 months for which product and package reliability has not been validated.
August 15, 2012Medical DevicesFDA
Smith & Nephew, Inc. Endoscopy Division recalls Smith & Nephew Dyonics Electroblade Resector, 4.5mm Full Radius Blade, BONECUTTER Part Number: 72202213 Product Usag
Hazard: Devices labeled with an expiry period of 48 months instead of 36 months; an additional 12 months for which product and package reliability has not been validated.