RecallRadar

FDA Device recall Z-2182-2012

Dimension(R) Reagent Management System (RMS) - Power Cord

On 2012-08-15 the FDA classified a Class II recall of Dimension(R) Reagent Management System (RMS) - Power Cord by Siemens Healthcare Diagnostics, citing siemens Healthcare Diagnostics has confirmed that partial insertion of the power cord on the Dimension Reagent Management System (RMS) power input module can cause the plug to ove….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2182-2012
ClassificationClass II
Statusterminated
Initiated2012-07-17
Published2012-08-15
Last updated2026-09-13 11:53 UTC
CompanySiemens Healthcare Diagnostics
DistributionAK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY

Product

Dimension(R) Reagent Management System (RMS) - Power Cord. The Siemens Healthcare Diagnostics Dimension(R) clinical chemistry analyzers are floor model, fully automated, microprocessor-controlled, integrated instrument systems that use prepackaged Flex(R) reagent test cartridges to measure a variety of analytes in human body fluids.

Reason

Siemens Healthcare Diagnostics has confirmed that partial insertion of the power cord on the Dimension Reagent Management System (RMS) power input module can cause the plug to overheat and potentially create a fire hazard. RMS without a power cord retention clip may be affected.

Identifiers

code_infoSerial numbers 99060001 - 99062554

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2182-2012%22

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