Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported March 15, 2017
Apollo EZ; Model: 9784152036 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures
Patient fell from the table because the footrest of the device detached from the table top while the patient was positioned on the table and table was moving from vertical positio…
Villa Sistemi Medicali S.p.a. recalled Apollo EZ; Model: 9784152036 Product Usage: General, multi-function x-ray systems cap… - a moderate-severity action.
Apollo EZ; Model: 9784152036 Product Usage: General, multi-function x-ray systems cap… was recalled by Villa Sistemi Medicali S.p.a. in March 15, 2017. Reason: Patient fell from the table because the footrest of the device detached from the table top while the patient …. Check the official notice for the remedy. Verify recall #Z-1430-2017 with the FDA Devices before acting.
The recall
Villa Sistemi Medicali S.p.a. issued this moderate-severity FDA Devices recall-Patient fell from the table because the footrest of the device detached from the table top while the patient ….
- Moderate
- severity level
- 65 units
- affected scope
- Class II
- classification
- March 15, 2017
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1430-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1430-2017) was formally reported on March 15, 2017, with the manufacturer initiating the action on December 27, 2016. It is classified under Moderate severity (Class II), with a current status of Terminated. Villa Sistemi Medicali S.p.a. is listed as the recalling firm, operating out of Buccinasco, N/A. Federal records list the affected scope as 65 devices in total.
The documented reason for this recall is: Patient fell from the table because the footrest of the device detached from the table top while the patient was positioned on the table and table was moving from vertical position. Distribution data in the federal record shows the product reached: US Nationwide distribution in the states of AL, AZ, CA, CO, CT, DC, FL, IA, IL, IN, LA, MA, MD, MI, MN, MO, MS, NJ, NY, PA, Puerto Rico, TN, TX, UT, and W.I. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
65 devices in total
Related Recalls
6
3 from same agency
Product description
Apollo EZ; Model: 9784152036 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures
Reason for recall
Patient fell from the table because the footrest of the device detached from the table top while the patient was positioned on the table and table was moving from vertical position.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1430-2017 |
| Date reported | March 15, 2017 |
| Date initiated | December 27, 2016 |
| Recalling firm | Villa Sistemi Medicali S.p.a. |
| Firm location | Buccinasco, N/A |
| Affected scope | 65 devices in total |
| Distribution | US Nationwide distribution in the states of AL, AZ, CA, CO, CT, DC, FL, IA, IL, IN, LA, MA, MD, MI, MN, MO, MS, NJ, NY, PA, Puerto Rico, TN, TX, UT, and W.I |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-1430-2017) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Apollo EZ; Model: 9784152036 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures. Recalled by Villa Sistemi Medicali S.p.a.. Units affected: 65 devices in total.
Why was this product recalled? ▼
Patient fell from the table because the footrest of the device detached from the table top while the patient was positioned on the table and table was moving from vertical position.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 15, 2017. Severity: Moderate. Recall number: Z-1430-2017.
Where was the recalled product distributed? ▼
Distribution: US Nationwide distribution in the states of AL, AZ, CA, CO, CT, DC, FL, IA, IL, IN, LA, MA, MD, MI, MN, MO, MS, NJ, NY, PA, Puerto Rico, TN, TX, UT, and W.I.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1430-2017) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported March 15, 2017. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.