Corentec Co recalls

Corentec Co has 3 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 12 Jun 2024. 2 are still ongoing. The most frequent reason is device malfunction.

Total recalls3since 2017

Last 12 months0reported

Class I00% of total

Ongoing2latest 12 Jun 2024

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 3 100%Class III 0 0%

Why corentec co is recalled

Device Malfunction267%
Other Reasons133%

Product types

By year

2024267%
2017133%

Ongoing corentec co recalls

2 active

Reported	Class	Recall	Company	Reason	Where
12 Jun 2024Device	CLASS II	Lospa Patella Component Model/Catalog Number: 01.10.9XX Software recalled	Corentec Co	Device Malfunction	Nationwide
12 Jun 2024Device	CLASS II	Tibial Insert recalled by Corentec Co	Corentec Co	Device Malfunction	Nationwide

All corentec co recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
12 Jun 2024Device	CLASS II	Lospa Patella Component Model/Catalog Number: 01.10.9XX Software recalled	Corentec Co	Device Malfunction	Nationwide
12 Jun 2024Device	CLASS II	Tibial Insert recalled by Corentec Co	Corentec Co	Device Malfunction	Nationwide
22 Mar 2017Device	CLASS II	Bencox Mirabo PE Liner 36/44 recalled by Corentec Co	Corentec Co	Other	PA

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.