Siemens recalls lab chemistry analyzer with risk of tubing cracks causing liquid leaks and slip hazards. Affected units have serial numbers A001 to M5295.
Flexible tubing connected to the liquid waste bottle can crack during routine customer maintenance potentially causing liquid waste can leak onto the floor, creating a slip and fall hazard
Siemens is recalling its IMMULITE 2000 XPi lab analyzers because flexible tubing can crack during maintenance, potentially leaking liquid waste and creating slip hazards. This affects lab equipment used in professional settings.
The flexible tubing connecting the liquid waste bottle can crack during routine maintenance. When this happens, liquid waste may leak onto floors, creating slip and fall hazards for people nearby.
Laboratory professionals using the IMMULITE 2000 XPi analyzers are most at risk. The recall applies to units with serial numbers A001 through M5295.
Check the serial number on the device, which ranges from A001 to M5295. The product is intended for professional laboratory use only.
Look for the serial number on the device, which should be between A001 and M5295.
The product is intended for professional laboratory use only. If the tubing cracks during maintenance, it could cause liquid leaks and slip hazards.
Check the serial number to see if it falls within A001 to M5295. If it does, contact Siemens Healthcare for guidance.
The affected units have serial numbers from A001 through M5295. The product is designed for professional laboratory environments only.
We’ve drafted a message you can send Siemens Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-2470-2020 — Siemens Healthcare Siemens Healthcare Hello, I own a Siemens Healthcare that is covered by recall Z-2470-2020 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.
