Corin Ltd

Complete recall history across all FDA and CPSC categories — 21 total recalls

Corin Ltd appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (21)

FDA medical device enforcement actions by Corin Ltd

Date Product Reason Class
Oct 13, 2023 Unity CR Femur Right, Size 6, Model Number 112.001.32 Primary and revisi... Potential for Unity CR Inserts Right size 6 from batch 529803 to be incorrect... Class II
Oct 13, 2023 Unity Total Knee System, Model Number 112.001.34. Primary and revision t... Potential for Unity CR Inserts Right size 6 from batch 529803 to be incorrect... Class II
Nov 8, 2022 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... Class II
Nov 8, 2022 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... Class II
Oct 31, 2022 Unity Total Knee System. Used for knee prosthesis in total knee replacement The internal packaging system for devices may have damage to the blisters pot... Class II
Jul 22, 2022 Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEM... One MetaFix size 7 collarless stem from batch 478179 which was incorrectly la... Class II
Jul 12, 2022 TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Ce... Some of the devices did not pass fatigue testing. Class II
Jul 28, 2021 Corin Trinity Screw, diameter 6.5mm 35mm Length, Cancellous Bone Screw, REF 3... The packaging system on the devices have potential physical and water damage ... Class II
Jul 28, 2021 Corin Trinity Dual Mobility, Size 4, Dual Mobility CoCr Liner, REF 321.04.540... The packaging system on the devices have potential physical and water damage ... Class II
Jul 28, 2021 Corin Trinity Liner ECIMA, diameter 40mm Neutral Offset, Taper Size 4, REF 3... The packaging system on the devices have potential physical and water damage ... Class II
Jul 28, 2021 Corin Trinity-i, diameter 50mm Taper Size 3, Non-Occluded Ti Plasma Shell, RE... The packaging system on the devices have potential physical and water damage ... Class II
Jul 28, 2021 Corin Unity Knee Augments, Size 5, 6 & 7 / 10mm Thick, Femoral Posterior Augm... The packaging system on the devices have potential physical and water damage ... Class II
Jul 28, 2021 Corin Unity Knee Patella, Size 3 / 8.5mm, Centered Dome 3 PEG-UHMWPE, REF 112... The packaging system on the devices have potential physical and water damage ... Class II
Jul 28, 2021 Corin TriFit TS, Size 8, Standard Tapered Stem, REF 694.0008, Sterile. The packaging system on the devices have potential physical and water damage ... Class II
Jul 28, 2021 Corin MetaFix Hip Stem, Size 1, Short Neck, 135 degrees, Collared Hip Stem, R... The packaging system on the devices have potential physical and water damage ... Class II
Jul 28, 2021 Corin BIOLOX Delta Mod Head, diameter 28mm Medium 0mm, 12/14 Taper, REF 104.2... The packaging system on the devices have potential physical and water damage ... Class II
Jul 28, 2021 Corin Unity Knee CS Insert, Size 5 / 9.0mm, Fixed Condylar Stabilised - UHMWP... The packaging system on the devices have potential physical and water damage ... Class II
May 6, 2021 Corin TriFit CF SIZE 7, LATERALISED 127o, COMBINED FIXATION STEM, CEMENTLESS,... Units from one batch of TriFit TS size 2 stem were found to be labeled as a T... Class II
May 6, 2021 Corin TriIFit TS SIZE 2, STANDARD TAPERED STEM, CEMENTLESS, REF 694.0002. Hi... Units from one batch of TriFit TS size 2 stem were found to be labeled as a T... Class II
Jan 25, 2021 Corin BIOLOX DELTA MOD HEAD 36mm EX LONG +8mm12/14 TAPER. Corin Trinity Aceta... The size indicated on the labeling on the outer packaging, on the inner packa... Class II
Jan 25, 2021 Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 TAPER. Corin Trinity Acet... The size indicated on the labeling on the outer packaging, on the inner packa... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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