--- title: "Corin Ltd Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Corin Ltd recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/corin-ltd/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Corin Ltd recall records **5** reported ongoing 7 records in this archive. Latest source date Oct 13, 2023. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Oct 13, 2023 FDA device enforcement ### [Unity CR Femur Right, Size 6, Model Number 112.001.32 Primary and revision total knee arthroplasty](https://isitonrecall.com/recall/fda-device-z-0213-2024-unity-cr-femur-right-size-6-model-number-112-001-32-primary-and-revision-total-knee-arthroplasty/) Potential for Unity CR Inserts Right size 6 from batch 529803 to be incorrectly labelled as Unity CR Inserts Right size 7 from batch 532405 and visa versa. Class II Reported ongoing Distribution: US: MI, TX, IL [Official source for Unity CR Femur Right, Size 6, Model Number 112.001.32 Primary and revision total knee arthroplasty](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0213-2024%22) Oct 13, 2023 FDA device enforcement ### [Unity Total Knee System, Model Number 112.001.34. Primary and revision total knee arthroplasty](https://isitonrecall.com/recall/fda-device-z-0214-2024-unity-total-knee-system-model-number-112-001-34-primary-and-revision-total-knee-arthroplasty/) Potential for Unity CR Inserts Right size 6 from batch 529803 to be incorrectly labelled as Unity CR Inserts Right size 7 from batch 532405 and visa versa. Class II Reported ongoing Distribution: US: MI, TX, IL [Official source for Unity Total Knee System, Model Number 112.001.34. Primary and revision total knee arthroplasty](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0214-2024%22) Nov 8, 2022 FDA device enforcement ### [Corin BIOLOX DELTA MOD HEAD,032mm, EX LONG +7mm, REF 104.3215](https://isitonrecall.com/recall/fda-device-z-0726-2023-corin-biolox-delta-mod-head-032mm-ex-long-7mm-ref-104-3215/) The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and vice-versa. Class II Reported ongoing Distribution: US Nationwide distribution in the states of FL, GA, MA, MI, Ok, PA, TX. [Official source for Corin BIOLOX DELTA MOD HEAD,032mm, EX LONG +7mm, REF 104.3215](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0726-2023%22) Nov 8, 2022 FDA device enforcement ### [Corin BIOLOX DELTA MOD HEAD, 036mm EX LONG +8mm, REF 104.3615](https://isitonrecall.com/recall/fda-device-z-0727-2023-corin-biolox-delta-mod-head-036mm-ex-long-8mm-ref-104-3615/) The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and vice-versa. Class II Reported ongoing Distribution: US Nationwide distribution in the states of FL, GA, MA, MI, Ok, PA, TX. [Official source for Corin BIOLOX DELTA MOD HEAD, 036mm EX LONG +8mm, REF 104.3615](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0727-2023%22) Oct 31, 2022 FDA device enforcement ### [Unity Total Knee System. Used for knee prosthesis in total knee replacement](https://isitonrecall.com/recall/fda-device-z-0273-2023-unity-total-knee-system-used-for-knee-prosthesis-in-total-knee-replacement/) The internal packaging system for devices may have damage to the blisters potentially damaging the device or compromising the sterility of the packaging. Class II Reported terminated Distribution: Distribution in the US to New Jersy and Puerto Rico. International distribution to South Africa and France. [Official source for Unity Total Knee System. Used for knee prosthesis in total knee replacement](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0273-2023%22) Jul 22, 2022 FDA device enforcement ### [Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number 579.0103](https://isitonrecall.com/recall/fda-device-z-1509-2022-corin-metafix-hip-stem-size-3-standard-135-degrees-collared-hip-stem-cementless-part-number-579-0103/) One MetaFix size 7 collarless stem from batch 478179 which was incorrectly labelled as a MetaFix size 3 collared stem from batch 485630. Class II Reported ongoing Distribution: US Nationwide distribution in the states of OK, TX, FL. [Official source for Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1509-2022%22) Jul 12, 2022 FDA device enforcement ### [TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip implant component.](https://isitonrecall.com/recall/fda-device-z-1667-2022-taperfit-stem-size-0-38mm-offset-12-14-taper-188-550-centraliser-for-cemented-use-ref-588-3800-ortho/) Some of the devices did not pass fatigue testing. Class II Reported terminated Distribution: Distribution was made to NJ. There was no military/government distribution. [Official source for TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588....](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1667-2022%22) ## Reasons in these listed records - Potential for Unity CR Inserts Right size 6 from batch 529803 to be incorrectly labelled as Unity CR Inserts Right size 7 from batch 532405 and visa versa. - The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and vice-versa. - The internal packaging system for devices may have damage to the blisters potentially damaging the device or compromising the sterility of the packaging. - One MetaFix size 7 collarless stem from batch 478179 which was incorrectly labelled as a MetaFix size 3 collared stem from batch 485630. These examples come from this result page and are not a ranking of every recall reason. ## Checking Corin Ltd ### Is there a recall on corin ltd right now? This archive contains 7 records, including 5 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Corin Ltd](https://isitonrecall.com/check/?q=Corin%20Ltd) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)