DePuy Mitek, Inc., a Johnson & Johnson recalls

DePuy Mitek, Inc., a Johnson & Johnson has 51 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 19 Mar 2025. 7 are still ongoing.

Total recalls51since 2012

Last 12 months0reported

Class I00% of total

Ongoing7latest 19 Mar 2025

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 2 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 51 100%Class III 0 0%

Why depuy mitek, inc., a johnson & johnson is recalled

Product types

By year

202524%
2023510%
201924%
201836%
2017510%
201636%
201512%
2013816%
20122243%

Ongoing depuy mitek, inc., a johnson & johnson recalls

7 active

Reported	Class	Recall	Company	Reason	Where
19 Mar 2025Device	CLASS II	COR Disposable Kit w/ Perpendicularity recalled	DePuy Mitek, Inc., a Johnson & Johnson	Other	Nationwide
19 Mar 2025Device	CLASS II	COR Disposable Kit Cartilage Transplant System recalled	DePuy Mitek, Inc., a Johnson & Johnson	Other	Nationwide
14 Jun 2023Device	CLASS II	DePuy Mitek Bioknotless Rapid w/ Pan-Indicated for use recalled	DePuy Mitek, Inc., a Johnson & Johnson	Device Malfunction	Nationwide
14 Jun 2023Device	CLASS II	DePuy Mitek Bioknotless Plus w/ Ethibond-Iindicated recalled	DePuy Mitek, Inc., a Johnson & Johnson	Device Malfunction	Nationwide
14 Jun 2023Device	CLASS II	DePuy Mitek Bioknotless Rapid W/ OC-Indicated for use recalled	DePuy Mitek, Inc., a Johnson & Johnson	Device Malfunction	Nationwide
14 Jun 2023Device	CLASS II	DePuy Mitek Bioknotless Plus w/ OC-Indicated for use recalled	DePuy Mitek, Inc., a Johnson & Johnson	Device Malfunction	Nationwide

All depuy mitek, inc., a johnson & johnson recalls, newest first

51 total

Reported	Class	Recall	Company	Reason	Where
19 Mar 2025Device	CLASS II	COR Disposable Kit w/ Perpendicularity recalled	DePuy Mitek, Inc., a Johnson & Johnson	Other	Nationwide
19 Mar 2025Device	CLASS II	COR Disposable Kit Cartilage Transplant System recalled	DePuy Mitek, Inc., a Johnson & Johnson	Other	Nationwide
14 Jun 2023Device	CLASS II	DePuy Mitek Bioknotless Rapid w/ Pan-Indicated for use recalled	DePuy Mitek, Inc., a Johnson & Johnson	Device Malfunction	Nationwide
14 Jun 2023Device	CLASS II	DePuy Mitek Bioknotless Plus w/ Ethibond-Iindicated recalled	DePuy Mitek, Inc., a Johnson & Johnson	Device Malfunction	Nationwide
14 Jun 2023Device	CLASS II	DePuy Mitek Bioknotless Rapid W/ OC-Indicated for use recalled	DePuy Mitek, Inc., a Johnson & Johnson	Device Malfunction	Nationwide
14 Jun 2023Device	CLASS II	DePuy Mitek Bioknotless Plus w/ OC-Indicated for use recalled	DePuy Mitek, Inc., a Johnson & Johnson	Device Malfunction	Nationwide
14 Jun 2023Device	CLASS II	DePuy Mitek Bioknotless Plus w/ Panacryl-Indicated recalled	DePuy Mitek, Inc., a Johnson & Johnson	Device Malfunction	Nationwide
18 Dec 2019Device	CLASS II	Healix Knotless ADV BR 5.5 Suture Anchor recalled	DePuy Mitek, Inc., a Johnson & Johnson	Other	24 states
18 Dec 2019Device	CLASS II	Healix Knotless ADV BR 4.75 Suture Anchor recalled	DePuy Mitek, Inc., a Johnson & Johnson	Other	24 states
31 Oct 2018Device	CLASS II	Mitek Screw and Washer Depth Gauge, Product recalled	DePuy Mitek, Inc., a Johnson & Johnson	Other	Nationwide
16 May 2018Device	CLASS II	Latarjet Experience Sharp Curved Ostetome recalled	DePuy Mitek, Inc., a Johnson & Johnson	Potency & Assay	Nationwide
7 Mar 2018Device	CLASS II	1113 Gravity Tube Set Pk/24 -SH recalled by DePuy Mitek, Inc., a Johnson	DePuy Mitek, Inc., a Johnson & Johnson	Packaging Defects	Nationwide
28 Jun 2017Device	CLASS II	DePuy Mitek Latarjet Experience Coracoid Top Hat Drill Product recalled	DePuy Mitek, Inc., a Johnson & Johnson	Device Malfunction	8 states
28 Jun 2017Device	CLASS II	DePuy Mitek Latarjet Experience-Combo Screw Driver Product recalled	DePuy Mitek, Inc., a Johnson & Johnson	Device Malfunction	8 states
28 Jun 2017Device	CLASS II	DePuy Mitek Latarjet Experience Top Hat Tap Product recalled	DePuy Mitek, Inc., a Johnson & Johnson	Device Malfunction	8 states
28 Jun 2017Device	CLASS II	DePuy Mitek Latarjet Experience Coracoid Drill Product recalled	DePuy Mitek, Inc., a Johnson & Johnson	Device Malfunction	8 states
28 Jun 2017Device	CLASS II	DePuy Mitek Latarjet Experience Extraction Driver Product recalled	DePuy Mitek, Inc., a Johnson & Johnson	Device Malfunction	8 states
27 Jan 2016Device	CLASS II	FMS neXtra¿ Full Radius Cutter Shaver Blades recalled	DePuy Mitek, Inc., a Johnson & Johnson	Labeling Errors	5 states
27 Jan 2016Device	CLASS II	FMS Ultra-Aggressive Cutter Shaver Blades recalled	DePuy Mitek, Inc., a Johnson & Johnson	Labeling Errors	5 states
27 Jan 2016Device	CLASS II	FMS neXtra¿ Aggressive Cutter Shaver Blades recalled	DePuy Mitek, Inc., a Johnson & Johnson	Labeling Errors	5 states
30 Dec 2015Device	CLASS II	Vapr¿ Tripolar 90" Degree Suction Electrodes recalled	DePuy Mitek, Inc., a Johnson & Johnson	Other	11 states
20 Nov 2013Device	CLASS II	DePuy Mitek FMS Outflow Tubing with One-Way valve Product recalled	DePuy Mitek, Inc., a Johnson & Johnson	Device Malfunction	Nationwide
20 Nov 2013Device	CLASS II	DePuy Mitek FMS Intermediary Tubing with One-Way valve Product recalled	DePuy Mitek, Inc., a Johnson & Johnson	Device Malfunction	Nationwide
15 May 2013Device	CLASS II	DePuy Mitek Tissue Liberator -Blade Up recalled	DePuy Mitek, Inc., a Johnson & Johnson	Other	KY, NJ
1 May 2013Device	CLASS II	Orthocord One Violet and One Blue Braided Composite Suture recalled	DePuy Mitek, Inc., a Johnson & Johnson	Labeling Errors	Nationwide
1 May 2013Device	CLASS II	Orthocord One Violet And One Blue Braided Composite Suture recalled	DePuy Mitek, Inc., a Johnson & Johnson	Labeling Errors	Nationwide
1 May 2013Device	CLASS II	Orthocord One Violet and One Blue Braided Composite Suture recalled	DePuy Mitek, Inc., a Johnson & Johnson	Labeling Errors	Nationwide
1 May 2013Device	CLASS II	Orthocord Blue Braided Composite Suture 2 (5 Metric) recalled	DePuy Mitek, Inc., a Johnson & Johnson	Labeling Errors	Nationwide
1 May 2013Device	CLASS II	Orthocord One Violet and One Blue Braided Composite Suture recalled	DePuy Mitek, Inc., a Johnson & Johnson	Labeling Errors	Nationwide
26 Dec 2012Device	CLASS II	DePuy Mitek Fully Fluted Reamer, Sterile Product Number recalled	DePuy Mitek, Inc., a Johnson & Johnson	Sterility	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.