Corin Recalls
21 recalls on record · March 31, 2021 to November 8, 2023 · Medical Devices
Recalls by year
21
22
23
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
November 8, 2023Medical DevicesFDA
Corin Ltd recalls Unity Total Knee System, Model Number 112.001.34. Primary and revision total knee arthroplasty
Hazard: 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.
November 8, 2023Medical DevicesFDA
Corin Ltd recalls Unity CR Femur Right, Size 6, Model Number 112.001.32 Primary and revision total knee arthroplasty
Hazard: 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.
December 28, 2022Medical DevicesFDA
Corin Ltd recalls Corin BIOLOX DELTA MOD HEAD, 036mm EX LONG +8mm, REF 104.3615
Hazard: The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and vice-versa.
December 28, 2022Medical DevicesFDA
Corin Ltd recalls Corin BIOLOX DELTA MOD HEAD,032mm, EX LONG +7mm, REF 104.3215
Hazard: The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and vice-versa.
November 30, 2022Medical DevicesFDA
Corin Ltd recalls Unity Total Knee System. Used for knee prosthesis in total knee replacement
Hazard: The internal packaging system for devices may have damage to the blisters potentially damaging the device or compromising the sterility of the packaging.
September 7, 2022Medical DevicesFDA
Corin Ltd recalls TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip i
Hazard: Some of the devices did not pass fatigue testing.
August 17, 2022Medical DevicesFDA
Corin Ltd recalls Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number 579.0103
Hazard: One MetaFix size 7 collarless stem from batch 478179 which was incorrectly labelled as a MetaFix size 3 collared stem from batch 485630.
October 6, 2021Medical DevicesFDA
Corin Ltd recalls Corin Unity Knee Patella, Size 3 / 8.5mm, Centered Dome 3 PEG-UHMWPE, REF 112.018.06, Sterile, a component of the Unity
Hazard: The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.
October 6, 2021Medical DevicesFDA
Corin Ltd recalls Corin Unity Knee CS Insert, Size 5 / 9.0mm, Fixed Condylar Stabilised - UHMWPE, REF 1125182, Sterile, and Corin Unity K
Hazard: The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.
October 6, 2021Medical DevicesFDA
Corin Ltd recalls Corin Unity Knee Augments, Size 5, 6 & 7 / 10mm Thick, Femoral Posterior Augment, REF 1122370, Sterile, a component of t
Hazard: The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.
October 6, 2021Medical DevicesFDA
Corin Ltd recalls Corin MetaFix Hip Stem, Size 1, Short Neck, 135 degrees, Collared Hip Stem, REF 579.0201, Sterile.
Hazard: The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.
October 6, 2021Medical DevicesFDA
Corin Ltd recalls Corin Trinity Dual Mobility, Size 4, Dual Mobility CoCr Liner, REF 321.04.540, Sterile, and Corin Dual Mobility, Size 4
Hazard: The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.
October 6, 2021Medical DevicesFDA
Corin Ltd recalls Corin BIOLOX Delta Mod Head, diameter 28mm Medium 0mm, 12/14 Taper, REF 104.2805, Sterile, a component of the Trinity Ac
Hazard: The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.
October 6, 2021Medical DevicesFDA
Corin Ltd recalls Corin Trinity Liner ECIMA, diameter 40mm Neutral Offset, Taper Size 4, REF 322.04.640, Sterile; and Corin Trinity Liner
Hazard: The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.
October 6, 2021Medical DevicesFDA
Corin Ltd recalls Corin Trinity-i, diameter 50mm Taper Size 3, Non-Occluded Ti Plasma Shell, REF 320.03.350, Sterile, a component of the T
Hazard: The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.
October 6, 2021Medical DevicesFDA
Corin Ltd recalls Corin Trinity Screw, diameter 6.5mm 35mm Length, Cancellous Bone Screw, REF 321.035, Sterile; and Corin Trinity Screw, d
Hazard: The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.
October 6, 2021Medical DevicesFDA
Corin Ltd recalls Corin TriFit TS, Size 8, Standard Tapered Stem, REF 694.0008, Sterile.
Hazard: The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.
June 23, 2021Medical DevicesFDA
Corin Ltd recalls Corin TriFit CF SIZE 7, LATERALISED 127o, COMBINED FIXATION STEM, CEMENTLESS, REF 6961007. Hip prosthesis component.
Hazard: Units from one batch of TriFit TS size 2 stem were found to be labeled as a TriFit CF size 7 stem. And vice versa.
June 23, 2021Medical DevicesFDA
Corin Ltd recalls Corin TriIFit TS SIZE 2, STANDARD TAPERED STEM, CEMENTLESS, REF 694.0002. Hip prosthesis component.
Hazard: Units from one batch of TriFit TS size 2 stem were found to be labeled as a TriFit CF size 7 stem. And vice versa.
March 31, 2021Medical DevicesFDA
Corin Ltd recalls Corin BIOLOX DELTA MOD HEAD 36mm EX LONG +8mm12/14 TAPER. Corin Trinity Acetabular System with Extra Long Heads/Trinity
Hazard: The size indicated on the labeling on the outer packaging, on the inner packaging, and on the patient stickers inside the packaging is incorrect: the Trinity Biolox Delta Ceramix Head 32XL is labeled as 36XL and vice-versa.
March 31, 2021Medical DevicesFDA
Corin Ltd recalls Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 TAPER. Corin Trinity Acetabular System with Extra Long Heads/Trinity
Hazard: The size indicated on the labeling on the outer packaging, on the inner packaging, and on the patient stickers inside the packaging is incorrect: the Trinity Biolox Delta Ceramix Head 32XL is labeled as 36XL and vice-versa.