Siemens Healthcare recalls STREAMLAB Refrigerated Storage Module 15000 units with potential pacemaker interference risk. Affected units may lack warning labels for pacemaker safety.
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
Siemens Healthcare is recalling its STREAMLAB Refrigerated Storage Module 15000 due to a potential risk of interference with pacemaker functionality. This could affect medical devices used by individuals with pacemakers.
The modules may have been shipped without a warning label that could interfere with pacemaker functionality. This risk exists because the device might cause unintended signals to medical implants.
Individuals with pacemakers who use the STREAMLAB Refrigerated Storage Module 15000 are most at risk. The recall affects medical device users who may have the module in their home or workplace.
Check for Siemens Healthcare STREAMLAB Refrigerated Storage Module 15000 units. The product has material numbers 10482428 and UDI 00630414949765. These units may lack a warning label for pacemaker safety.
Look for a warning label indicating pacemaker interference risk on the module.
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
The recall record does not specify a remedy, so check for a warning label and contact Siemens Healthcare for guidance.
Check for Siemens Healthcare STREAMLAB Refrigerated Storage Module 15000 with material numbers 10482428 and UDI 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-0217-2019 — Siemens Healthcare Siemens Healthcare Hello, I own a Siemens Healthcare that is covered by recall Z-0217-2019 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.
