Tranberg MR Cannula, REF: 4013-05, Rx Only, Sterile EO - Product Usage: used with the Tranberg¿ M...
FDA Device Recall #Z-1780-2021 — Class II — April 1, 2021
Recall Summary
| Recall Number | Z-1780-2021 |
| Classification | Class II — Moderate risk |
| Date Initiated | April 1, 2021 |
| Status | Terminated |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | CLINICAL LASERTHERMIA SYSTEMS AB |
| Location | Lund |
| Product Type | Devices |
| Quantity | 40 units |
Product Description
Tranberg MR Cannula, REF: 4013-05, Rx Only, Sterile EO - Product Usage: used with the Tranberg¿ MR Introducer; a device used to aid the insertion of the Laser Applicator into the tissue.
Reason for Recall
single use devices labeled as sterile may not have been adequately sterilized
Distribution Pattern
Worldwide distribution - US Nationwide distribution in the states of TX, MD, CA and the countries of Canada, Germany, Switzerland.
Lot / Code Information
Lot ID: 116539201117 and 116539030718 M
Other Recalls from CLINICAL LASERTHERMIA SYSTEMS AB
| Recall # | Classification | Product | Date |
|---|---|---|---|
| Z-1781-2021 | Class II | Tranberg MR Stylet, 1.8mm/15G, 230mm, REF: 4013... | Apr 1, 2021 |
| Z-1782-2021 | Class II | Tranberg Laser Applicator Non-cooled, 1.7mm/ 15... | Apr 1, 2021 |
Frequently Asked Questions
Sterility recalls for medical devices vary in severity. If you have already had a procedure using a potentially non-sterile device, contact your healthcare provider immediately — you may need monitoring for signs of infection. Symptoms to watch for include fever, redness or swelling at the surgical site, unusual pain, or discharge. For devices that have not yet been used, they should be quarantined and returned to the manufacturer per the recall notice. Non-sterile implants can cause serious infections; early detection and treatment are critical.
Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.
Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.
What Should You Do?
Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.