Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported October 12, 2016
Panoramic X-ray Model PC-1000, Laser-1000 packed in a crate Product Usage: The PC-1000 will enable the user to take panoramic x-ray images. The PC-1000/Laser1000 will enable the user to take panoramic x-ray images as well as cephalometric x-ray images.
Panoramic Corporation is performing a voluntary Medical Device Correction on certain PC-1000 X-ray systems due to the potential for a safety nut to be ineffective, which could res…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Panoramic Rental Corp. recalled Panoramic X-ray Model PC-1000, Laser-1000 packed in a crate Product Usage: The PC-100… - a moderate-severity action.
Panoramic X-ray Model PC-1000, Laser-1000 packed in a crate Product Usage: The PC-100… was recalled by Panoramic Rental Corp. in October 12, 2016. Reason: Panoramic Corporation is performing a voluntary Medical Device Correction on certain PC-1000 X-ray systems du…. Check the official notice for the remedy. Verify recall #Z-0016-2017 with the FDA Devices before acting.
The recall
Panoramic Rental Corp. issued this moderate-severity FDA Devices recall-Panoramic Corporation is performing a voluntary Medical Device Correction on certain PC-1000 X-ray systems du….
- Moderate
- severity level
- 13K units
- affected scope
- Class II
- classification
- October 12, 2016
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0016-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0016-2017) was formally reported on October 12, 2016, with the manufacturer initiating the action on August 19, 2016. It is classified under Moderate severity (Class II), with a current status of Terminated. Panoramic Rental Corp. is listed as the recalling firm, operating out of Fort Wayne, IN. Federal records list the affected scope as 13,340.
The documented reason for this recall is: Panoramic Corporation is performing a voluntary Medical Device Correction on certain PC-1000 X-ray systems due to the potential for a safety nut to be ineffective, which could result in blunt force trauma that may impac… Distribution data in the federal record shows the product reached: US Nationwide Distribution including Puerto Rico. 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
13,340
Related Recalls
6
3 from same agency
Product description
Panoramic X-ray Model PC-1000, Laser-1000 packed in a crate Product Usage: The PC-1000 will enable the user to take panoramic x-ray images. The PC-1000/Laser1000 will enable the user to take panoramic x-ray images as well as cephalometric x-ray images.
Reason for recall
Panoramic Corporation is performing a voluntary Medical Device Correction on certain PC-1000 X-ray systems due to the potential for a safety nut to be ineffective, which could result in blunt force trauma that may impact the head, neck or shoulders.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0016-2017 |
| Date reported | October 12, 2016 |
| Date initiated | August 19, 2016 |
| Recalling firm | Panoramic Rental Corp. |
| Firm location | Fort Wayne, IN |
| Affected scope | 13,340 |
| Distribution | US Nationwide Distribution including Puerto Rico |
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-0016-2017) 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? ▼
Panoramic X-ray Model PC-1000, Laser-1000 packed in a crate Product Usage: The PC-1000 will enable the user to take panoramic x-ray images. The PC-1000/Laser1000 will enable the user to take panoramic x-ray images as well as cephalometric x-ray images.. Recalled by Panoramic Rental Corp.. Units affected: 13,340.
Why was this product recalled? ▼
Panoramic Corporation is performing a voluntary Medical Device Correction on certain PC-1000 X-ray systems due to the potential for a safety nut to be ineffective, which could result in blunt force trauma that may impact the head, neck or shoulders.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 12, 2016. Severity: Moderate. Recall number: Z-0016-2017.
Where was the recalled product distributed? ▼
Distribution: US Nationwide Distribution including Puerto Rico.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0016-2017) 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 October 12, 2016. 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.