Surge Cardiovascular recalls Retrograde Cardioplegia Cannula Model RMG-0015S due to rigid stylet design potentially causing injury during use.
The device was built with the rigid insertion stylet instead of the flexible stylet.
Surge Cardiovascular is recalling Retrograde Cardioplegia Cannula Model RMG-0015S because it was built with a rigid stylet instead of a flexible one. This could cause injury during medical procedures. The recall affects medical devices used in heart surgery.
The device uses a rigid stylet instead of a flexible one, which could cause injury during insertion into the heart. This design flaw might lead to complications during cardioplegia procedures.
Healthcare professionals using the device for heart surgery are most at risk. The recall applies to specific medical devices sold for cardiac procedures.
Check for the model number RMG-0015S on the device. The recall applies to devices with lot code 00794-030718.
Look for the model number RMG-0015S on the device.
Contact Surge Cardiovascular for specific instructions on how to proceed with the recall.
The model number is RMG-0015S.
The device was built with a rigid stylet instead of a flexible one, which could cause injury during use.
Check the model number and contact Surge Cardiovascular for specific instructions.
We’ve drafted a message you can send Surge Cardiovascular to request your refund or repair — edit it as you like.
Subject: Recall Z-0068-2019 — Surge Cardiovascular Surge Cardiovascular Hello, I own a Surge Cardiovascular that is covered by recall Z-0068-2019 from Surge Cardiovascular. 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.
