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DePuy Mitek, Inc., a Johnson & Johnson Recalls
51 recalls on record · July 11, 2012 to March 19, 2025 · 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.
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls SpiraLok 6.5 w/out Needles with violet and blue Orthocord Product Number: 222988 SPIRALOK Anchors are primarily used
Hazard: Fracture of SPIRALOK Anchors post op, requiring patient revision
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls SpiraLok 6.5 w/Needles with violet and blue Orthocord Product Number: 222987 SPIRALOK Anchors are primarily used to
Hazard: Fracture of SPIRALOK Anchors post op, requiring patient revision
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls SpiraLok 5.0 w/out Needles with violet and blue Orthocord Product Number: 222986 SPIRALOK Anchors are primarily used
Hazard: Fracture of SPIRALOK Anchors post op, requiring patient revision
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls SpiraLok 5.0 w/Needles with violet and blue Orthocord Product Number: 222985 SPIRALOK Anchors are primarily used to
Hazard: Fracture of SPIRALOK Anchors post op, requiring patient revision
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls SpiraLok 6.5 w/out Needles with Orthocord Product Number: 222971 SPIRALOK Anchors are primarily used to re-attach so
Hazard: Fracture of SPIRALOK Anchors post op, requiring patient revision
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls SpiraLok 6.5 w/Needles with Orthocord Product Number: 222970 SPIRALOK Anchors are primarily used to re-attach soft t
Hazard: Fracture of SPIRALOK Anchors post op, requiring patient revision
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls SpiraLok 5.0 w/out Needles with Orthocord Product Number: 222969 SPIRALOK Anchors are primarily used to re-attach so
Hazard: Fracture of SPIRALOK Anchors post op, requiring patient revision
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls SpiraLok 5.0 w/Needles with Orthocord Product Number: 222968 SPIRALOK Anchors are primarily used to re-attach soft t
Hazard: Fracture of SPIRALOK Anchors post op, requiring patient revision
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls Screw, fixation, boneProduct Number: 222967 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in r
Hazard: Fracture of SPIRALOK Anchors post op, requiring patient revision
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls SpiraLok 6.5mm with Ethibond without needles Product Number: 222966 SPIRALOK Anchors are primarily used to re-attach
Hazard: Fracture of SPIRALOK Anchors post op, requiring patient revision
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls SpiraLok 5.0mm with Panacryl without needles Product Number: 222965 SPIRALOK Anchors are primarily used to re-attach
Hazard: Fracture of SPIRALOK Anchors post op, requiring patient revision
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls SpiraLok 5.0mm with Ethibond without needles Product Number: 222964 SPIRALOK Anchors are primarily used to re-attach
Hazard: Fracture of SPIRALOK Anchors post op, requiring patient revision
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls SpiraLok 6.5mm with Panacryl and needles Product Number: 222963 SPIRALOK Anchors are primarily used to re-attach sof
Hazard: Fracture of SPIRALOK Anchors post op, requiring patient revision
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls SpiraLok 6.5mm with Ethibond and needles Product Number: 222962 SPIRALOK Anchors are primarily used to re-attach sof
Hazard: Fracture of SPIRALOK Anchors post op, requiring patient revision
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls SpiraLok 5.0mm with Panacryl and needles Product Number: 222961 SPIRALOK Anchors are primarily used to re-attach sof
Hazard: Fracture of SPIRALOK Anchors post op, requiring patient revision
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls SpiraLok 5.0mm with Ethibond and needles Product Number: 222960 SPIRALOK Anchors are primarily used to re-attach sof
Hazard: Fracture of SPIRALOK Anchors post op, requiring patient revision
October 31, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls DePuy Mitek VAPR Hook Electrode 3.5mm Hook Electrode with Integrated Handpiece Catalog Number: 227305 The DePuy M
Hazard: Product may have wrong large product identification label with symbols on the box indicating a S90 VAPR Electrode instead of the VAPR 3.5 hook electrode
July 11, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls Depuy Spine Side Fire Needles 13G X 4IN Side-Fire Needle, part of the Confidence Spinal Cement System Product Code 2839
Hazard: Additional Instructions for Use and Surgical Technique for the Confidence Needle due to reports of breakage with the side fire needles
July 11, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls Depuy Spine Side Fire Needles 11G X 6IN Side-Fire Needle, part of the Confidence Spinal Cement System Product Code 283
Hazard: Additional Instructions for Use and Surgical Technique for the Confidence Needle due to reports of breakage with the side fire needles
July 11, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls Depuy Spine Side Fire Needles 11G X 4IN, part of the Confidence Spinal Cement System Product Code: 283904411. The Co
Hazard: Additional Instructions for Use and Surgical Technique for the Confidence Needle due to reports of breakage with the side fire needles
July 11, 2012Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls Depuy Spine Side Fire Needles 13G X 6IN, part of the Confidence Spinal Cement System Product Code 283904613. The Co
Hazard: Additional Instructions for Use and Surgical Technique for the Confidence Needle due to reports of breakage with the side fire needles