Cerapedics recalls specific bone graft syringes due to incorrect part numbers on labels. Patients may receive wrong product amounts. No action needed as labels are not the product itself.
Patient chart label contains incorrect Part Number and volume amount.
Cerapedics is recalling certain bone graft syringes because their labels have incorrect part numbers and volume amounts. This could lead to patients getting the wrong product amount during medical procedures. No action is needed since the labels don't affect the product's safety.
The patient chart label shows the wrong part number and volume amount. This could mean a patient receives the incorrect product amount during medical procedures. However, the labels do not affect the syringe's physical safety.
Patients using Cerapedics i-FACTOR Bone Graft syringes with model 700-010 may be affected. Medical professionals handling these syringes are most at risk of administering incorrect product amounts.
Check for the model number 700-010 on the syringe label. The lot number is 21C0991. This product was sold with the UDI code (01)00850001680004(17)240531(10)21C0991.
Verify the syringe label for model number 700-010 and lot number 21C0991.
No action is needed. The labels do not affect the product's safety.
The recall record states the label has an incorrect part number, but does not specify the correct one.
Check for model number 700-010 and lot number 21C0991 on the syringe label.
We’ve drafted a message you can send Cerapedics to request your refund or repair — edit it as you like.
Subject: Recall Z-1056-2022 — Cerapedics Cerapedics Hello, I own a Cerapedics that is covered by recall Z-1056-2022 from Cerapedics. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
