In2bones USA recalls NeoSpan SuperElastic Compression Staples due to missing Magnetic Resonance Conditional symbol on packaging and labels. This could lead to unsafe MRI scans if used without proper labeling.
Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.
In2bones USA is recalling NeoSpan SuperElastic Compression Staples because the carton, inner tray, and patient labels lack the required Magnetic Resonance Conditional symbol. This means the staples might not be safe for MRI scans, potentially causing injury during medical procedures.
The missing Magnetic Resonance Conditional symbol means the staples may not be safe for MRI scans. If a patient with these staples undergoes an MRI, the staples could heat up and cause burns or other injuries.
Medical professionals using these staples for bone fixation procedures are most at risk. Patients undergoing MRI scans after using these staples could face safety issues.
Check for the product names 'NeoSpan SuperElastic Compression Staple w/Instruments' with catalog numbers T50 SN010, T50 SN012, T50 SN020, T50 SN110, T50 SN115, or T50 SN118. The UDI-DI codes are listed in the recall notice.
Look for the Magnetic Resonance Conditional symbol on the carton, inner tray, and patient label. If missing, the product is recalled.
The recall is due to the missing Magnetic Resonance Conditional symbol on the carton, inner tray, and patient label, which could lead to unsafe MRI scans.
Check if the product has the required Magnetic Resonance Conditional symbol. If missing, stop using it and contact In2bones USA for further instructions.
No, the missing symbol means these staples may not be safe for MRI scans, potentially causing injury during the procedure.
We’ve drafted a message you can send In2bones to request your refund or repair — edit it as you like.
Subject: Recall Z-2355-2026 — In2bones In2bones Hello, I own a In2bones that is covered by recall Z-2355-2026 from In2bones. 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.
