Ziehm Imaging Inc
Ziehm Imaging Inc has 3 FDA enforcement events on this register (14 product records) between 2013 and 2017: 3 device; the busiest year was 2013 with 1.
0% of its events are Class I; the most common class is Class II (3). 0 events are listed as ongoing; the recalling firm's address is in FL.
Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.
Enforcement events
| Initiated | Product (first record) | Type | Class | Records | Status |
|---|---|---|---|---|---|
| 23 Feb 2017 | Ziehm Imaging solo FD Mobile Fluoroscopic C-arm | Device | Class II | 1 | Terminated |
| 15 Apr 2016 | Ziehm Vision RFD 3D Mobile C-arm for Mobile Fluoroscopic Imaging | Device | Class II | 6 | Terminated |
| 21 Nov 2013 | Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging | Device | Class II | 7 | Terminated |
By type and class
Class I: 0% of this firm's events; 18% of all events on the register.
Events by year
Questions and answers
How many FDA recalls has Ziehm Imaging Inc had?
3 enforcement events (14 product records) on this register, 2013–2017: 3 device.
Are any Ziehm Imaging Inc recalls ongoing?
0 events are listed as ongoing in the current openFDA export.
What class are Ziehm Imaging Inc recalls?
3 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.
Where does this data come from?
openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.
Provenance
Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.