Siemens Healthcare recalls Dimension EXL 200 and related models due to single-insulated motor cables that could cause electrical shock. Affected units include specific model numbers and serial ranges. No remedy is provided in the recall notice.
Thermal chamber motors have electrical cables with single insulation rather than the required double insulation. There is no exposed current due to the single insulation that could result in a potential electrical shock
Siemens Healthcare is recalling Dimension Thermal Chamber Motor Cables in certain models because they have single insulation instead of double insulation. This could potentially cause electrical shock if the cable is damaged. The recall includes specific model numbers and serial ranges.
The motor cables in these devices have single insulation instead of the required double insulation. While the recall states there is no exposed current that could result in shock, the single insulation could become damaged, potentially leading to electrical shock if the cable is compromised.
Users of Siemens Dimension EXL 200 and related models with specific model numbers and serial ranges are affected. Laboratory technicians and medical professionals using these instruments are most at risk due to potential electrical hazards.
Check for model numbers and serial numbers listed in the recall notice. Affected models include Dimension EXL 200, Dimension EXL with LM, Dimension EXL with LM with STM, and other variants with specific UDI numbers. Serial numbers start with patterns like 221106, 973106, or 223948-X.
Compare your device's model number and serial number against the list provided in the recall notice to determine if it is affected.
The motor cables have single insulation instead of double insulation, which could potentially lead to electrical shock if the cable is damaged.
The recall notice does not provide a remedy, so no action is required beyond checking if your device is affected.
Affected models include Dimension EXL 200, Dimension EXL with LM, Dimension EXL with LM with STM, and other variants with specific UDI numbers listed in the recall notice.
We’ve drafted a message you can send Siemens Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0409-2019 — Siemens Healthcare Siemens Healthcare Hello, I own a Siemens Healthcare that is covered by recall Z-0409-2019 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.
