United Orthopedic recalls

United Orthopedic has 12 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 12 Aug 2026. 9 are still ongoing. 6 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls12since 2017

Last 12 months6reported

Class I00% of total

Ongoing9latest 12 Aug 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 0 0Nov 0 0 0Feb 0 0 0May 0 0 6Aug 0 0

Severity split

Class I 0 0%Class II 12 100%Class III 0 0%

Why united orthopedic is recalled

Product types

Hip & Knee Implants1083%
Heart & Vascular Devices217%

By year

2026650%
2024325%
2018217%
201718%

Ongoing united orthopedic recalls

9 active

Reported	Class	Recall	Company	Reason	Where
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

All united orthopedic recalls, newest first

12 total

Reported	Class	Recall	Company	Reason	Where
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
6 Mar 2024Device	CLASS II	Ustar II Knee System Cemented curved stem, RHS recalled	United Orthopedic	Other	9 states
6 Mar 2024Device	CLASS II	Ustar II Hip System Press-Fit Curved Stem recalled by United Orthopedic	United Orthopedic	Other	9 states
6 Mar 2024Device	CLASS II	Ustar II Knee System : Cemented Curved Stem recalled	United Orthopedic	Other	9 states
28 Mar 2018Device	CLASS II	U2 Total Knee System Tibial Insert, PSA, #1 Thick recalled	United Orthopedic	Packaging Defects	N/A
28 Mar 2018Device	CLASS II	U2 Total Knee System Tibial Insert, Posterior Stabilized, #3 Thick recalled	United Orthopedic	Packaging Defects	N/A
5 Apr 2017Device	CLASS II	UOC Femoral Driver, Product number PE recalled by United Orthopedic	United Orthopedic	Device Malfunction	CA

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.