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FDA (Device enforcement)Recalled 2017-05-11closedclass ii

GE Medical Systems, LLC: Signa PET/MR (K163619, K142098) Product Usage: The SIGNA PET/MR system combines magnetic resonance diagnostic devices (MRDD) and Positron Emission Tomography (PET) scanners th

Is my product affected?

Signa PET/MR (K163619, K142098) Product Usage: The SIGNA PET/MR system combines magnetic resonance diagnostic devices (MRDD) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information, acquired simultaneously and isoce

  • UPC 00840682115971
  • UPC 00840682115872
  • UPC 00840682103817
  • UPC 00840682105699
  • UPC 840682105378

Check against the official notice below — it lists the full affected range.

What happened

GE Medical Systems is recalling 68 units of its SIGNA PET/MR system, a combined magnetic resonance and positron emission tomography scanner used for medical imaging. The recall affects devices distributed nationwide across 22 states including California, Texas, New York, Pennsylvania, Florida, and others. The reason for the recall is possible incorrect wiring of the Uninterruptable Power Supply, which could create a potential electrical shock hazard.

The affected devices are identified by multiple medical device listing numbers and model numbers provided in the recall documentation. The record does not specify a remedy for consumers who may have affected units.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Possible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potential shock hazard.

Details from the source

Reason for recall: Possible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potential shock hazard. Distribution: US Nationwide in the states of : AK, CA, CO, CT, DE, FL, IA, IL, IN, KS, KY, LA, MD, MO, ND, NE, NJ, NY, OH, PA, TX, WA, and WI Quantity: 68 units in total Lot/code info: Medical Device Listing No. D117354, D295466, D182389, D102432, D206140, D230310, D269569, D102430, D140572, D188736, D102434, D234841, D196247, D134019, D236543, D006275, D159181, D288890, D229859; Model No. Eaton 9130, 5323286, 5396502-5, 5499460-3, 5499460-6, 5499460-9, 5741000-3, 00840682115971, 5396502-2, 5499460-2, 5741000-2, 00840682115872, 5373011-3, 5396469-3, 5481490-2, 5481500-7, 5499460-7, 5499460-10, 5741000, 00840682103817, 5323286-101, 2377062-61, 2395001, 2395001-2, 2395001-3, 2395001-4, 00840682105699, 840682105378

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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