DePuy Spine recalls EIT CIF cage implants due to potential label mismatch between outer carton and blister packages. This may cause confusion in identifying the correct product for spinal fusion procedures.
Label on the Outer Carton does not match the labels on the Outer Blister package, Inner Blister package and Patient Labels. The only label that may not be correct is on the Outer Carton
DeP: Spine recalls specific spinal fusion implants because the outer carton label might not match the inner package labels. This mismatch could lead to using the wrong product during surgery.
The outer carton label may not match the labels on the inner blister packages or patient labels. This mismatch could lead to using the wrong implant during spinal fusion surgery, potentially causing complications.
Patients who received the EIT CIF cage implants with part number CUI8070S or lot number E20CL0637 are affected. Surgeons and medical staff using these implants for spinal fusion procedures are most at risk.
Check for part number CUI8070S and lot number E20CL0637 on the outer carton, blister packages, and patient labels. The product is used for spinal fusion in cervical disc disease cases.
Verify the outer carton label matches the inner blister package and patient labels for part number CUI8070S and lot number E20CL0637.
The recall is happening because the outer carton label may not match the labels on the inner blister packages or patient labels, which could lead to using the wrong implant during surgery.
Check if your product has part number CUI8070S and lot number E20CL0637. If it does, verify the labels match before use.
The recall indicates a potential label mismatch that could lead to using the wrong implant, but the official notice does not specify a risk of serious injury.
We’ve drafted a message you can send DePuy Spine to request your refund or repair — edit it as you like.
Subject: Recall Z-1324-2022 — DePuy Spine DePuy Spine Hello, I own a DePuy Spine that is covered by recall Z-1324-2022 from DePuy Spine. 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.
