Panoramic X-ray Model PC-1000 Recalled for Jackscrew Nut Failure
Panoramic Rental Corp. is recalling 7,885 Panoramic X-ray Model PC-1000 units due to a jackscrew nut part failure that could cause device malfunction and injury.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II and involves a structural defect (jackscrew nut failure) that poses a risk of injury to patients and operators, meeting the criteria for a Severe rating.
Plain-English summary
Panoramic Rental Corp. is recalling 7,885 units of the Panoramic X-ray Model PC-1000 and PC-1000/Laser 1000. These devices are used to take panoramic and cephalometric x-ray images. The recall is due to a jackscrew nut part failure that may lead to device malfunction and potential injury to patients or operators.
The affected units have Model Numbers 800724-1 and 800724-3, with Serial Numbers ranging from 6001 to 13885. These devices were manufactured between 1996 and 2003. The recall covers units distributed worldwide, including all 50 U.S. states, Puerto Rico, and numerous international locations.
Users of these devices should stop using them and contact the recalling firm for instructions on repair or replacement.
The recalled product
- Product
- Panoramic X-ray Model PC-1000 The PC-1000 will enable the user to take panoramic x-ray images. The PC-1000/Laser 1000 will enable the user to take panoramic x-ray images as well as cephalometric x-ray images.
- Manufacturer
- Panoramic Rental Corp.
- Hazard
- Affected units
- 7,885
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- Model Number: 800724-1
- 800724-3
- Serial Numbers 6001 to 13885
- Manufactured Between 1996 and 2003
Distribution
Related recalls
Same manufacturer · Panoramic Rental Corp.
See all →- HighPanoramic PC-1000 Dental X-ray Units Recalled for Lift Motor Wear
FDA (Devices) · 2018-02-14
- HighPanoramic PC-1000 X-ray Systems Recalled for Safety Nut Defect
FDA (Devices) · 2016-10-12
Same hazard · mechanical failure
See all →- HighIMRIS ORT300 Operating Room Table Recalled for Mechanical Failure Risk
FDA (Devices) · 2026-09-02
- HighIMRIS ORT200 Operating Room Table Recalled for Mechanical Failure Risk
FDA (Devices) · 2026-09-02
- HighForest River Transit Buses Recalled for Wheelchair Lift Control Failure
NHTSA · 2026-09-01
- HighBlue Bird Recalls Vision School Buses Due to Wheelchair Lift Defect
NHTSA · 2026-08-31
- SevereMagic Tilt Watercraft Trailers Recalled Due to Winch Weld Failure
NHTSA · 2026-08-28