OrthoPediatrics recalls Model 01-1501-0032 Child Nail Attachment Bolt due to potential binding with intramedullary nails, which may delay surgical procedures. Affected units sold in specific regions.
Binding can occur between the attachment bolt and intramedullary nail, which may lead to delays in surgical procedures.
OrthoPediatrics is recalling a specific child nail attachment bolt used in pediatric orthopedic surgery. Binding between this bolt and the intramedullary nail could delay surgery, so affected users should contact the company for details.
The attachment bolt can bind with the intramedullary nail during surgery, potentially causing delays in the procedure. This is a mechanical issue that may not cause injury but could impact surgical timing.
Pediatric orthopedic surgeons and hospitals using the recalled bolt for children's surgical implants. The risk is low as binding is unlikely to cause injury but may delay procedures.
Check for the model number 01-1501-0032 on the bolt. The product was sold in specific regions with serial numbers starting with 173265-A through 192431-B.
Reach out to OrthoPediatrics for specific instructions on the recalled bolt model and how to proceed.
The recall is for potential binding that may delay surgery, but it does not pose a risk of injury. The hazard is low risk as it does not cause harm directly.
Check for the model number 01-1501-0032 on the bolt. The product was sold with serial numbers starting with 173265-A through 192431-B.
Contact OrthoPediatrics for specific instructions on the recalled bolt model and how to proceed.
We’ve drafted a message you can send OrthoPediatrics to request your refund or repair — edit it as you like.
Subject: Recall Z-0218-2020 — OrthoPediatrics OrthoPediatrics Hello, I own a OrthoPediatrics that is covered by recall Z-0218-2020 from OrthoPediatrics. 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.
