Siemens Healthcare recalls STREAMLAB Refrigerated Storage Module 9000 units that may lack pacemaker warning labels, risking interference with medical devices. Affected units have specific Siemens material numbers and UDI codes.
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
Siemens Healthcare is recalling refrigerated storage modules for their STREAMLAB system because some units might not have warning labels that could interfere with pacemakers. This means the device might cause issues for people with pacemakers if not properly labeled.
The refrigerated storage modules may have been shipped without a warning label that could interfere with pacemaker function. This means the device might cause unintended signals to pacemakers, potentially leading to health issues if not properly labeled.
People with pacemakers or implanted medical devices who use the STREAMLAB system are most at risk. The recall affects specific Siemens Healthcare product models sold with certain material numbers and UDI codes.
Check for Siemens Material Numbers: 10482426, 10464532, or 10635930. Also look for the UDI code 00630414949765 on the product.
Ensure the module has a warning label about pacemaker interference before use.
The recall does not require immediate stop use; check for the warning label first.
The official notice does not specify a remedy, so contact Siemens Healthcare directly for guidance.
Check for Siemens Material Numbers: 10482426, 10464532, or 10635930, and UDI code 00630414949765.
We’ve drafted a message you can send Siemens Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0216-2019 — Siemens Healthcare Siemens Healthcare Hello, I own a Siemens Healthcare that is covered by recall Z-0216-2019 from Siemens Healthcare. 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.
