PlainRecalls
FDA Devices Moderate Class II Ongoing

Osstem Dental X-Ray System T2. Product Model Numbers T2-C and T2-CS.

Reported: November 12, 2025 Initiated: August 26, 2025 #Z-0314-2026

Product Description

Osstem Dental X-Ray System T2. Product Model Numbers T2-C and T2-CS.

Reason for Recall

Osstem Implant Co. Ltd, is voluntarily initiating a medical device correction involving the current labeling for this electronic product may be missing a required Certification Statement under 21 CFR Subchapter J (Radiological Health Regulations). Specifically, the following statement may have been omitted: Certification Statement: This electronic product complies with all applicable performance standards prescribed under 21 CFR Subchapter J, as enforced by the U.S. Food and Drug Administration at the date of manufacturing.

Details

Recalling Firm
OSSTEM Implant Co., Ltd.
Units Affected
N/A
Distribution
U.S.
Location
Haeundae District, N/A

Frequently Asked Questions

What product was recalled?
Osstem Dental X-Ray System T2. Product Model Numbers T2-C and T2-CS.. Recalled by OSSTEM Implant Co., Ltd.. Units affected: N/A.
Why was this product recalled?
Osstem Implant Co. Ltd, is voluntarily initiating a medical device correction involving the current labeling for this electronic product may be missing a required Certification Statement under 21 CFR Subchapter J (Radiological Health Regulations). Specifically, the following statement may have been omitted: Certification Statement: This electronic product complies with all applicable performance standards prescribed under 21 CFR Subchapter J, as enforced by the U.S. Food and Drug Administration at the date of manufacturing.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 12, 2025. Severity: Moderate. Recall number: Z-0314-2026.