Device recall: SIGNA Premier nuclear magnetic resonance imaging system
Class II FDA enforcement event 88665. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Under certain conditions, some slices may be missing which can lead to a gap of anatomy in the 3D Volume images.
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
GE Healthcare, LLC started this device recall on 26 Aug 2021. The firm address in the FDA record is in Waukesha, WI. FDA put the recall in Class II. FDA event 88665 has 10 product records. The first FDA enforcement report date is 27 Oct 2021. The record gives the status Terminated, with the termination date 4 May 2026.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
Distribution in United States to AZ, CA, FL, GA, IL, LA, MA, MD, MN, NC, NH, NJ, NY, OH, OK, TX, VA, WA, and Puerto Rico OUS distribution to: Australia, Belgium, Canada, Chile, Colombia, France,…
Recalling firm
GE Healthcare, LLC, Waukesha, WI.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
10 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-0132-2022 | SIGNA Premier nuclear magnetic resonance imaging system | 11 devices | Class II | Terminated | 27 Oct 2021 |
| Z-0133-2022 | SIGNA Architect nuclear magnetic resonance imaging system | 2 devices | Class II | Terminated | 27 Oct 2021 |
| Z-0134-2022 | SIGNA Pioneer nuclear magnetic resonance imaging system | 5 devices | Class II | Terminated | 27 Oct 2021 |
| Z-0135-2022 | Discovery MR750w 3.0T nuclear magnetic resonance imaging system | 13 devices | Class II | Terminated | 27 Oct 2021 |
| Z-0136-2022 | Discovery MR750 3.0T nuclear magnetic resonance imaging system | 5 devices | Class II | Terminated | 27 Oct 2021 |
| Z-0137-2022 | SIGNA Creator, SIGNA Explorer nuclear magnetic resonance imaging system | 6 devices | Class II | Terminated | 27 Oct 2021 |
| Z-0138-2022 | SIGNA Voyager nuclear magnetic resonance imaging system | 15 devices | Class II | Terminated | 27 Oct 2021 |
| Z-0139-2022 | SIGNA Artist nuclear magnetic resonance imaging system | 18 devices | Class II | Terminated | 27 Oct 2021 |
| Z-0140-2022 | Optima MR450w 1.5T nuclear magnetic resonance imaging system | 13 devices | Class II | Terminated | 27 Oct 2021 |
| Z-0141-2022 | 1.5T SIGNA HDxt MR System nuclear magnetic resonance imaging system | 3 devices | Class II | Terminated | 27 Oct 2021 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Device events that started in 2021
- 900
- Share of these events in Class II
- 89%
- Product records in this event
- 10Median of the firm: 1
- Events of the firm on the register
- 225
Other events of the firm
Official channels
- FDA enforcement report Z-0132-2022The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
Follow by RSS:Food, drug and device recallsFDA Class I recalls
Cite this page
Recall Register. FDA enforcement event 88665. https://recallregister.com/fda/ii/88665/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA device enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
Distribution in United States to AZ, CA, FL, GA, IL, LA, MA, MD, MN, NC, NH, NJ, NY, OH, OK, TX, VA, WA, and Puerto Rico OUS distribution to: Australia, Belgium, Canada, Chile, Colombia, France,…
- What quantity of product is in FDA event 88665?
- The event has 10 product records. The first record gives this quantity:
11 devices
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many device recalls of 2021 have the same class?
- 89% of the 900 device events that started in 2021 are in Class II.