Smith & Nephew, Inc. Endoscopy Division: 37 recalls on record

Recalls filed with 1 agency: FDA (37).

First recall on record: August 15, 2012. Most recent: July 23, 2014.

Risk classification: Class II: 37

Most recent recalls

DateAgencyProduct
September 25, 2013FDATWINFIX ULTRA PLLA/HA 5.5 mm Suture Anchor with 3 ULTRABRAID Suture: Part Number: 7220260…Z-2234-2013
September 25, 2013FDATWINFIX" Ultra 4.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures (blue, blue-CO…Z-2238-2013
September 25, 2013FDAOSTEORAPTOR CURVED 2.3 mm Suture Anchor ULTRABRAID COBRAID Suture, Black; Part Number: 7…Z-2227-2013
September 25, 2013FDABIORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID Suture; Part Number: 72200774 Biodegr…Z-2216-2013
September 25, 2013FDATWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture, Blue / Black; Part Number…Z-2230-2013
September 25, 2013FDATWINFIX Ultra 6.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures (blue, blue-COB…Z-2240-2013
August 15, 2012FDASmith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures(white, COBRAID-blue), s…Z-2166-2012
August 15, 2012FDASmith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with three #2 sutures (white, COBRAID- blue…Z-2168-2012
August 15, 2012FDASmith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures (COBRAID-blue, COBRAIDb…Z-2167-2012
August 15, 2012FDASmith & Nephew 5.5 mm Dyonics Bonecutter ,Electroblade Full Radius Part Number: 720596…Z-2145-2012
August 15, 2012FDASmith & Nephew Dyonics Electroblade Resector, 4.5mm Full Radius Blade, BONECUTTER Part N…Z-2144-2012
August 15, 2012FDASmith & Nephew 5.5 mm TWINFIX Ultra Ti Suture Anchor with two #2 ULTRABRAID sutures (blue…Z-2165-2012

Questions about this company

How many recalls does Smith & Nephew, Inc. Endoscopy Division have?
Recalert has 37 U.S. recalls on record for Smith & Nephew, Inc. Endoscopy Division, published between August 15, 2012 and July 23, 2014.
Which agencies have handled Smith & Nephew, Inc. Endoscopy Division recalls?
Smith & Nephew, Inc. Endoscopy Division appears as the recalling firm in recalls from: FDA (37).

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