Corin Ltd recalls
Every recall we track for Corin Ltd — 21 in all, from 2021–2023 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Corin Ltd peaked in 2021 (14); 21 since 2017.
All FDA recall records for Corin Ltd since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 14 | 0 | 14 |
| 2022 | 0 | 0 | 5 | 0 | 5 |
| 2023 | 0 | 0 | 2 | 0 | 2 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Corin Ltd product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Corin Ltd recalls
8 shown- Lower riskMedical device
Corin Ltd recalls Unity Total Knee System, Model Number 112.001.34. Primary and revision total knee arthroplasty
Corin recalls Unity Total Knee System model 112.001.34 with batch numbers 529803-532405 due to potential incorrect labeling of knee implant sizes.
CorinOct 13, 2023 - Lower riskMedical device
Corin Ltd recalls Corin BIOLOX DELTA MOD HEAD, 036mm EX LONG +8mm, REF 104.3615
Corin recalls BIOLOX Delta ceramic heads with size labeling error that may cause incorrect fit. Affected units have size 36XL labeled as 32XL and vice versa.
CorinNov 8, 2022 - Lower riskMedical device
Corin Ltd recalls Unity Total Knee System. Used for knee prosthesis in total knee replacement
Corin recalls Unity Total Knee System (Model 112.040.06) due to potential packaging damage risking device sterility. Affected patients should contact Corin for guidance.
CorinOct 31, 2022 - Lower riskMedical device
Corin Ltd recalls Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number 579.0103
Corin recalls specific hip stem models due to incorrect labeling that could lead to improper use. Affected units have batch numbers 485630. Consumers should verify their product details.
CorinJul 22, 2022 - Lower riskMedical device
Corin Ltd recalls TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip
Corin recalls orthopedic hip implant component TaperFit Stem (REF 588.3800) due to failure in fatigue testing. Affected units may not withstand repeated use without failure.
CorinJul 12, 2022 - Lower riskMedical device
Corin Ltd recalls Corin Unity Knee CS Insert, Size 5 / 9.0mm, Fixed Condylar Stabilised - UHMWPE, REF 1125182, Sterile, and Corin Unity
Corin recalls specific knee implant components due to packaging issues that may cause device damage or contamination. Affected units shipped between July 22-26, 2021. Contact Corin for details.
CorinJul 28, 2021 - Lower riskMedical device
Corin Ltd recalls Corin TriIFit TS SIZE 2, STANDARD TAPERED STEM, CEMENTLESS, REF 694.0002. Hip prosthesis component.
Corin recalls hip prosthesis components with incorrect size labels that could lead to improper fitting. Affected units have a specific lot number and model.
CorinMay 6, 2021 - Lower riskMedical device
Corin Ltd recalls Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 TAPER. Corin Trinity Acetabular System with Extra Long
Corin recalls hip prostheses with incorrect size labeling on packaging, risking improper fit. Affected units have Trinity Biolox Delta Ceramix heads labeled as 36XL instead of 32XL. Consumers should contact Corin for details.
CorinJan 25, 2021
Corin Ltd recall questions
How many recalls has Corin Ltd had?
21 recalls from Corin Ltd are on record with U.S. safety agencies, from 2021–2023.
What is the most recent Corin Ltd recall?
Corin Ltd recalls Unity Total Knee System, Model Number 112.001.34. Primary and revision total knee arthroplasty, dated Oct 13, 2023. Every Corin Ltd recall is listed on this page, newest first.
What should I do if I have a recalled Corin Ltd product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Corin Ltd recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.