Device recall: Ziehm Vision RFD 3D Mobile C-arm for Mobile Fluoroscopic Imaging
Class II FDA enforcement event 74013. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Malfunction of the radiation-warning timer and the 3D-specific interval warning. No 5-minute timer dialogs or beeper will occur until the unit is rebooted.
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
Ziehm Imaging Inc started this device recall on 15 Apr 2016. The firm address in the FDA record is in Orlando, FL. FDA put the recall in Class II. FDA event 74013 has 6 product records. The first FDA enforcement report date is 31 Aug 2016. The record gives the status Terminated, with the termination date 18 Jul 2019.
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.
US Distribution including Puerto Rico and to the states of :FL, GA, VA,MA. ME, MI, NY, NJ, PA, RI, IL, TX, AZ, CA, NV, UT, and WA.
Recalling firm
Ziehm Imaging Inc, Orlando, FL.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
6 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-2639-2016 | Ziehm Vision RFD 3D Mobile C-arm for Mobile Fluoroscopic Imaging | 31 devices | Class II | Terminated | 31 Aug 2016 |
| Z-2640-2016 | Ziehm Vision RFD Mot, Mobile C-arm for Mobile Fluoroscopic Imaging | 14 devices | Class II | Terminated | 31 Aug 2016 |
| Z-2641-2016 | Ziehm Vision RFD, Mobile C-arm for Mobile Fluoroscopic Imaging | 2 devices | Class II | Terminated | 31 Aug 2016 |
| Z-2642-2016 | Ziehm Vision R, Mobile C-arm for Mobile Fluoroscopic Imaging | 1 device | Class II | Terminated | 31 Aug 2016 |
| Z-2643-2016 | Ziehm Solo, Mobile C-arm for Mobile Fluoroscopic Imaging | 12 devices | Class II | Terminated | 31 Aug 2016 |
| Z-2644-2016 | Ziehm Vision2, Mobile C-arm for Mobile Fluoroscopic Imaging | 2 devices | Class II | Terminated | 31 Aug 2016 |
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 2016
- 1,232
- Share of these events in Class II
- 91%
- Product records in this event
- 6Median of the firm: 6
- Events of the firm on the register
- 3
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 23 Feb 2017 | Ziehm Imaging solo FD Mobile Fluoroscopic C-arm | Device | Class II | 1 |
| 21 Nov 2013 | Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging | Device | Class II | 7 |
Official channels
- FDA enforcement report Z-2639-2016The 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.
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Cite this page
Recall Register. FDA enforcement event 74013. https://recallregister.com/fda/ii/74013/. 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:
US Distribution including Puerto Rico and to the states of :FL, GA, VA,MA. ME, MI, NY, NJ, PA, RI, IL, TX, AZ, CA, NV, UT, and WA.
- What quantity of product is in FDA event 74013?
- The event has 6 product records. The first record gives this quantity:
31 devices
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many device recalls of 2016 have the same class?
- 91% of the 1,232 device events that started in 2016 are in Class II.