Corin Ltd

FDA recalling firm · 8 enforcement events · 21 product records · 2021–2023 · N/A

Corin Ltd has 8 FDA enforcement events on this register (21 product records) between 2021 and 2023: 8 device; the busiest year was 2022 with 4.

0% of its events are Class I; the most common class is Class II (8). 3 events are listed as ongoing; the recalling firm's address is in N/A.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

Initiated	Product (first record)	Type	Class	Records	Status
13 Oct 2023	Unity CR Femur Right, Size 6, Model Number 112.001.32 Primary and revision total knee arthroplasty	Device	Class II	2	Ongoing
8 Nov 2022	Corin BIOLOX DELTA MOD HEAD,032mm, EX LONG +7mm, REF 104.3215	Device	Class II	2	Ongoing
31 Oct 2022	Unity Total Knee System. Used for knee prosthesis in total knee replacement	Device	Class II	1	Terminated
22 Jul 2022	Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number 579.0103	Device	Class II	1	Ongoing
12 Jul 2022	TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip implant component.	Device	Class II	1	Terminated
28 Jul 2021	Corin TriFit TS, Size 8, Standard Tapered Stem, REF 694.0008, Sterile.	Device	Class II	10	Terminated
6 May 2021	Corin TriIFit TS SIZE 2, STANDARD TAPERED STEM, CEMENTLESS, REF 694.0002. Hip prosthesis component.	Device	Class II	2	Terminated
25 Jan 2021	Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 TAPER. Corin Trinity Acetabular System with Extra Long Heads/Trinity Biolox Delta Ceramic Head (Generic Name: Hip Prosthesis). The Trinity Acetabular System is a modular acetabular cup system consisting of a press fit, titanium alloy shell; acetabular liners in…	Device	Class II	2	Terminated

By type and class

Device8

Class II8

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

Enforcement events for Corin Ltd by year initiated.

Questions and answers

How many FDA recalls has Corin Ltd had?

8 enforcement events (21 product records) on this register, 2021–2023: 8 device.

Are any Corin Ltd recalls ongoing?

3 events are listed as ongoing in the current openFDA export.

What class are Corin Ltd recalls?

8 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.