Panoramic X-ray Model PC-1000 — Class II medical device recall Z-0016-2017
Terminated recall by Panoramic Rental Corp., reported 2016-10-12, distributed nationwide. Panoramic Corporation is performing a voluntary Medical Device Correction on certain PC-1000 X-ray systems due
| Recall number | Z-0016-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Panoramic Rental Corp., Fort Wayne, IN, United States |
| Recall initiated | 2016-08-19 |
| Classified | 2016-10-03 |
| Reported by FDA | 2016-10-12 |
| Terminated | 2018-01-11 |
| Distributed | Nationwide (US) |
| Quantity | 13,340 |
| Serial numbers | 19340, 6001 |
| Model numbers | 800724-1, 800724-3, LASER-1000, PC-1000 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0016-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.