DePuy Spine recalls EIT CIF cage implants due to potential label mismatch between outer carton and blister packages. Affected units may have incorrect labeling, but no safety hazard is reported. Consumers should check product details and contact DePuy for verification.
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
DePuy Spine is recalling EIT CIF cage spinal implants because the outer carton label may not match the inner blister or patient labels. This mismatch could lead to confusion about the product's specifications, but there is no stated risk of injury or malfunction.
The outer carton label may not match the inner blister or patient labels, potentially causing confusion about the product's specifications. However, the recall does not indicate any safety hazard or injury risk.
Patients who received EIT CIF cage implants with part number CUI8060L for cervical disc disease. Those most at risk are individuals using the product without verifying the labels.
Check for part number CUI806: EIT CIF cage, H 6mm, 8degree, L- for cervical disc disease. The product was sold with lot number E20CL0603. Labels on the outer carton should match the inner blister and patient labels.
Verify that the outer carton label matches the inner blister and patient labels for part number CUI8060L.
The recall states there is no safety hazard or injury risk reported.
Contact DePuy Spine directly to confirm your product details and follow their instructions.
The recall does not indicate any safety hazard, but label verification is recommended.
We’ve drafted a message you can send DePuy Spine to request your refund or repair — edit it as you like.
Subject: Recall Z-1323-2022 — DePuy Spine DePuy Spine Hello, I own a DePuy Spine that is covered by recall Z-1323-2022 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.
