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All product recalls associated with Nobel Biocare Vastra Hamngatan 1 Goteborg Sweden.
Total Recalls
1000
Past Year
620
Class I (Serious)
91
Most Recent
Dec 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Due to manufacturing issue (unintended by-product of the injection molding process) a sharp pin that may puncture the blister packaging and breaching the sterile barrier of the finished product.
Product complaints were received describing the A820 myPTM app taking longer than expected for patients to interact with their implantable pump.
The MSOT Acuity Echo does not include an adequate instruction for safe operation of the device. The previous version of the user manuals contained a wrong value for the Nominal Ocular Hazard Distance (NOHD).