Hip & Knee Implants recalls

3,110 medical device recalls in the hip & knee implants category are on file with the FDA, from 2012 to 30 Sep 2026.

Total recalls3,110since 2012

Last 12 months101reported

Class I512% of total

Ongoing647latest 30 Sep 2026

Recalls per month, last 24 months

click a bar for that month

14Nov '24 4 9 4Feb 6 21 9May 7 11 3Aug 5 9 7Nov 18 3 5Feb 1 4 10May 5 17 9Aug 14 0

Severity split

Class I 51 2%Class II 3,036 98%Class III 23 1%

Why hip & knee implants is recalled

Companies

By year

2026682%
20251094%
20242067%
20231575%
2022873%
20211595%
20202137%
20191936%
201860019%
20172267%

Ongoing hip & knee implants recalls

647 active

Reported	Class	Recall	Company	Reason	Where
30 Sep 2026Device	CLASS II	Trinity Non-Surgical Isolation Gown, AAMI PB70 Level 2, X-Large recalled	New York Embroidery Studio	Packaging Defects	Nationwide
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

All hip & knee implants recalls, newest first

3,110 total

Reported	Class	Recall	Company	Reason	Where
30 Sep 2026Device	CLASS II	Trinity Non-Surgical Isolation Gown, AAMI PB70 Level 2, X-Large recalled	New York Embroidery Studio	Packaging Defects	Nationwide
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
2 Sep 2026Device	CLASS II	Medline convenience kits labeled as: Femoral Pack, Medline Kit recalled	Medline Industries	Other	Nationwide
26 Aug 2026Device	CLASS II	Arvis Surgical Navigation System Gen recalled by Kico Knee Innovation	Kico Knee Innovation	Device Malfunction	19 states
26 Aug 2026Device	CLASS II	Veritas Standard Reverse Total Shoulder Veritas Standard recalled	restor3d	Device Malfunction	Nationwide
19 Aug 2026Device	CLASS II	Endo-Model, Replacement Set, Tibial Plateau, right/left, L, Uhmwpe recalled	Waldemar Link GmbH & Co. KG (Mfg Site)	Other	IN
12 Aug 2026Device	CLASS II	U2 Total Knee System Femoral offset bushing recalled	United Orthopedic	Device Malfunction	Nationwide
12 Aug 2026Device	CLASS II	U2 Total Knee System Femoral valgus offset adaptor, left recalled	United Orthopedic	Device Malfunction	Nationwide
12 Aug 2026Device	CLASS II	Ustar II Knee System Hinge Box Trial, L, #1 recalled	United Orthopedic	Device Malfunction	Nationwide
12 Aug 2026Device	CLASS II	U2 Total Knee System PSA Box Trial, L, #1 recalled by United Orthopedic	United Orthopedic	Device Malfunction	Nationwide
12 Aug 2026Device	CLASS II	U2 Total Knee System Femoral offset bushing recalled	United Orthopedic	Device Malfunction	Nationwide
12 Aug 2026Device	CLASS II	U2 Total Knee System Femoral valgus adaptor, left and right recalled	United Orthopedic	Device Malfunction	Nationwide
29 Jul 2026Device	CLASS I	Medline convenience kits labeled as: Total Joint Kit, Medline Kit recalled	Medline Industries	Other	8 states
29 Jul 2026Device	CLASS I	Medline medical procedure convenience kit labeled as recalled	Medline Industries	Other	CO, IL
29 Jul 2026Device	CLASS I	Medline Anterior Hip, Medline Kit recalled by Medline Industries	Medline Industries	Other	8 states
29 Jul 2026Device	CLASS I	Medline medical procedure convenience kit labeled as recalled	Medline Industries	Other	CO, IL
22 Jul 2026Device	CLASS II	Medline Kits containing Zimmer Biomet mixing bowls recalled	Medline Industries	Sterility	Nationwide
22 Jul 2026Device	CLASS II	Orthofix Minirail, Short, Lengthener recalled by Orthofix U.S	Orthofix U.S	Labeling Errors	22 states
22 Jul 2026Device	CLASS II	Orthofix Minirail, Articulated, Fixator, Vertical Axis recalled	Orthofix U.S	Labeling Errors	22 states

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.