Every recall we track for Corin Ltd — 21 in all — plus the complaints and injury reports the public filed about them.
Corin recalls Unity CR Femur Right Size 6 implants with potential labeling errors between sizes 6 and 7. Affected units may be mislabeled, requiring verification of batch numbers.
Corin recalls Unity Total Knee System model 112.001.34 with batch numbers 529803-532405 due to potential incorrect labeling of knee implant sizes.
Corin recalls BIOLOX DELTA MOD HEADs with size labels swapped. This labeling error may cause incorrect sizing for medical use. Affected units have specific model numbers and lot codes.
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.
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.
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.
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.
Corin recalls specific bone screws due to packaging that may cause water damage, loss of sterility, or contamination. Affected products shipped between July 22-26, 2021.
Corin recalls specific size 4 dual mobility implants due to packaging issues that could cause contamination or loss of sterility. Affected units shipped between July 22-26, 2021.
Corin recalls specific Trinity Liner ECIMA implants due to packaging issues that may cause water damage, loss of sterility, or contamination. Affected units were shipped between July 22-26, 2021.
Corin recalls specific Trinity-i hip implants (REF 320.03.350) delivered 7/22-26/2021 due to packaging that may cause water damage, loss of sterility, or contamination.
Corin recalls Unity Knee Augments (Size 5-7, 10mm thick) due to packaging risks that could cause contamination or loss of sterility. Affected units shipped between July 22-26, 2021.
Corin recalls specific Unity Knee Patella components (size 3/8.5mm) delivered 7/22-26/2021 due to packaging risks causing contamination or loss of sterility. Affected units may require replacement.
Corin recalls specific TriFit TS surgical implants due to packaging issues that could cause contamination or loss of sterility. Affected units shipped between July 22-26, 2021, with lot number 467870.
Corin recalls specific hip stem implants due to packaging issues that could cause contamination or loss of sterility. Affected units shipped between July 22-26, 2021, with lot number 476399 delivered July 22-23, 2021.
Corin recalls specific BIOLOX Delta Mod Head components due to packaging issues that could cause water damage, loss of sterility, or contamination. Affected units shipped between July 22-26, 2021.
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.
Corin recalls hip prosthesis components labeled incorrectly as size 7 when they are size 2, potentially causing improper fit. Affected units have lot number 467881.
Corin recalls hip prosthesis components with incorrect size labels that could lead to improper fitting. Affected units have a specific lot number and model.
Corin recalls hip prostheses with incorrect size labels on packaging. The Trinity Biolox Delta Ceramix head is labeled as 36mm instead of 32mm, risking improper fit and complications.
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.
