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.
One MetaFix size 7 collarless stem from batch 478179 which was incorrectly labelled as a MetaFix size 3 collared stem from batch 485630.
Corin is recalling certain hip stem implants because they were incorrectly labeled. This could lead to improper surgical use if the wrong size is installed. Affected products have specific batch numbers and part numbers.
The hip stem was mislabeled as a size 3 collared stem when it was actually a size 7 collarless stem. This mismatch could cause improper surgical fitting if the wrong size is used during implantation.
Patients who received hip implants with the specific batch number 485630 and part number 579.0103 are most at risk. This applies to individuals who had surgery using the incorrectly labeled stems.
Check the product label for part number 579.0103 and batch number 485630. The UDI code includes the batch number 485630 in the sequence.
Check the product label for part number 579.0103 and batch number 485630 to confirm if your hip stem is affected.
The hip stem was incorrectly labeled as a size 3 collared stem when it was actually a size 7 collarless stem, which could lead to improper surgical use.
Check the product label for part number 579.0103 and batch number 485630. The UDI code includes the batch number 485630 in the sequence.
The recall does not specify a remedy, so you should verify your product details to determine if it is affected.
We’ve drafted a message you can send Corin to request your refund or repair — edit it as you like.
Subject: Recall Z-1509-2022 — Corin Corin Hello, I own a Corin that is covered by recall Z-1509-2022 from Corin. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
