Howmedica Osteonics recalls

Howmedica Osteonics has 244 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 23 Sep 2026. 122 are still ongoing. 16 were reported in the last 12 months.

Total recalls244since 2016

Last 12 months16reported

Class I00% of total

Ongoing122latest 23 Sep 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 1 0Nov 1 0 0Feb 1 0 0May 2 0 0Aug 12 0

Severity split

Class I 0 0%Class II 242 99%Class III 2 1%

Why howmedica osteonics is recalled

Product types

By year

2026156%
202521%
20248836%
202352%
2022125%
202152%
2020187%
201983%
20188836%
201631%

Ongoing howmedica osteonics recalls

122 active

Reported	Class	Recall	Company	Reason	Where
23 Sep 2026Device	CLASS II	Axle Pin Assy Large Elbow Cobalt Chrome recalled by Howmedica Osteonics	Howmedica Osteonics	Other	Nationwide
23 Sep 2026Device	CLASS II	Triathlon Hinge Insert Size 4 5612-p-411 Triathlon Hinge recalled	Howmedica Osteonics	Other	Nationwide
23 Sep 2026Device	CLASS II	Scorpio Recessed Metal Backed Patella 3045 recalled	Howmedica Osteonics	Foreign Material	Nationwide
23 Sep 2026Device	CLASS II	Bearing And Axle Bushing Assy Std Elbow C-m113-1-301 Krh recalled	Howmedica Osteonics	Other	Nationwide
23 Sep 2026Device	CLASS II	Scorpio + Mobile Bearing Pcs 78-5-0910 System One Bipolar recalled	Howmedica Osteonics	Other	Nationwide
23 Sep 2026Device	CLASS II	Duracon XL Angled Tib Ins C-m064-1-300 Self-pressurizing recalled	Howmedica Osteonics	Other	Nationwide

All howmedica osteonics recalls, newest first

244 total

Reported	Class	Recall	Company	Reason	Where
23 Sep 2026Device	CLASS II	Axle Pin Assy Large Elbow Cobalt Chrome recalled by Howmedica Osteonics	Howmedica Osteonics	Other	Nationwide
23 Sep 2026Device	CLASS II	Triathlon Hinge Insert Size 4 5612-p-411 Triathlon Hinge recalled	Howmedica Osteonics	Other	Nationwide
23 Sep 2026Device	CLASS II	Scorpio Recessed Metal Backed Patella 3045 recalled	Howmedica Osteonics	Foreign Material	Nationwide
23 Sep 2026Device	CLASS II	Bearing And Axle Bushing Assy Std Elbow C-m113-1-301 Krh recalled	Howmedica Osteonics	Other	Nationwide
23 Sep 2026Device	CLASS II	Scorpio + Mobile Bearing Pcs 78-5-0910 System One Bipolar recalled	Howmedica Osteonics	Other	Nationwide
23 Sep 2026Device	CLASS II	Duracon XL Angled Tib Ins C-m064-1-300 Self-pressurizing recalled	Howmedica Osteonics	Other	Nationwide
23 Sep 2026Device	CLASS II	All Poly Constrained Insert 69-2854 Nrg Knee Cr recalled	Howmedica Osteonics	Other	Nationwide
23 Sep 2026Device	CLASS II	Trident 0¿ Poly Insert ID 620-00-28D Orthopaedic implant recalled	Howmedica Osteonics	Other	Nationwide
23 Sep 2026Device	CLASS II	Omnifit Series I Acet recalled by Howmedica Osteonics	Howmedica Osteonics	Other	Nationwide
23 Sep 2026Device	CLASS II	Acetabular Cup Uhmwpe 61-3258 All Poly Constrained Insert recalled	Howmedica Osteonics	Other	Nationwide
23 Sep 2026Device	CLASS II	Abg I Acetabular Insert Hooded Id C-m079-2-801 Arc2f recalled	Howmedica Osteonics	Other	Nationwide
23 Sep 2026Device	CLASS II	Scorpio C-dome Patella 73-2710 73-2910 Scorpio U-dome recalled	Howmedica Osteonics	Other	Nationwide
24 Jun 2026Device	CLASS II	Tri Ts Baseplate Size recalled by Howmedica Osteonics	Howmedica Osteonics	Packaging Defects	Nationwide
24 Jun 2026Device	CLASS II	Tri Ts Baseplate Size recalled by Howmedica Osteonics	Howmedica Osteonics	Packaging Defects	Nationwide
25 Mar 2026Device	CLASS II	MICS3 Angled Sagittal Saw Attachment recalled by Howmedica Osteonics	Howmedica Osteonics	Other	Nationwide
31 Dec 2025Device	CLASS II	The Stryker CranialMask Tracker is a single-use device recalled	Howmedica Osteonics	Device Malfunction	Nationwide
8 Oct 2025Device	CLASS II	Exeter V40 Stem No recalled by Howmedica Osteonics	Howmedica Osteonics	Packaging Defects	NJ
16 Oct 2024Device	CLASS II	Triathlon Universal TS Baseplate Size recalled by Howmedica Osteonics	Howmedica Osteonics	Potency & Assay	Nationwide
16 Oct 2024Device	CLASS II	Mako Integrated Cutting System (Mics) Handpiece recalled	Howmedica Osteonics	Other	Nationwide
4 Sep 2024Device	CLASS II	Custom Made Device - Gmrs Extension Piece Left recalled	Howmedica Osteonics	Other	NJ
24 Jul 2024Device	CLASS II	Unitrax Endoprosthesis Head Component recalled by Howmedica Osteonics	Howmedica Osteonics	Labeling Errors	Nationwide
24 Jul 2024Device	CLASS II	Unitrax Endoprosthesis Head Component recalled by Howmedica Osteonics	Howmedica Osteonics	Labeling Errors	Nationwide
24 Jul 2024Device	CLASS II	Unitrax Endoprosthesis Head Component recalled by Howmedica Osteonics	Howmedica Osteonics	Labeling Errors	Nationwide
26 Jun 2024Device	CLASS II	HRIS Storage & Sterilization Case and Tray recalled	Howmedica Osteonics	Sterility	Nationwide
26 Jun 2024Device	CLASS II	Gray Revision Instrument System Accessory Tray/Case recalled	Howmedica Osteonics	Sterility	Nationwide
1 May 2024Device	CLASS II	Tridentii Hemi CLUSTER54E- Indicated for use in primary recalled	Howmedica Osteonics	Other	Nationwide
1 May 2024Device	CLASS II	Tridentii Hemi CLUSTER44B- Indicated for use in primary recalled	Howmedica Osteonics	Other	Nationwide
1 May 2024Device	CLASS II	Tridentii PSL CLUSTER50D- Indicated for use in primary recalled	Howmedica Osteonics	Other	Nationwide
1 May 2024Device	CLASS II	Tridentii Hemi CLUSTER58F- Indicated for use in primary recalled	Howmedica Osteonics	Other	Nationwide
1 May 2024Device	CLASS II	Tridentii Hemi CLUSTER52E-Indicated for use in primary recalled	Howmedica Osteonics	Other	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.