Nobel Biocare Usa Llc NobelReplace Conical Connection RP 4.3x11.5 mm REF 36707 STERILE R Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
NobelReplace Conical Connection RP 4.3x11.5 mm REF 36707 STERILE R
Brand
Nobel Biocare Usa Llc
Lot Codes / Batch Numbers
Catalog Number: 36707 UDI Code: (01)07332747160529(10)13116495(11)210720(17)260618, (01)07332747160529(10)13116496(11)210720(17)260618, (01)07332747160529(10)13116497(11)210720(17)260618, Lot Numbers: 13116495, 13116496, 13116497
Products Sold
Catalog Number: 36707 UDI Code: (01)07332747160529(10)13116495(11)210720(17)260618; (01)07332747160529(10)13116496(11)210720(17)260618; (01)07332747160529(10)13116497(11)210720(17)260618; Lot Numbers: 13116495, 13116496, 13116497
Nobel Biocare Usa Llc is recalling NobelReplace Conical Connection RP 4.3x11.5 mm REF 36707 STERILE R due to Due to 16 complaints related to drivers not engaging in implants. According to the firm's investigations, the incorrect offset gauge was potentially . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Due to 16 complaints related to drivers not engaging in implants. According to the firm's investigations, the incorrect offset gauge was potentially used during production of the implants. As a result, this could potentially lead to aborted or a delay in surgical procedure.
Recommended Action
Per FDA guidance
On 01/12/2022, the firm sent an "URGENT MEDICAL DEVICE RECALL" Letter via UPS to customers informing them that specific batches/lots of devices, the dimensions of the hexagon connection part are potentially not fully conforming to specification and may not fully engage in the implant. Customers are instructed to: 1. Inspect their stock and quarantine all affected devices. 2. Complete the Customer Acknowledgement Form and return to the Recalling Firm via email or fax within 5 days of receipt of this notice. 3. Return all affected stock on hand to the Recalling Firm using the shipping label provided. 4. Ensure relevant staff members are informed of this recall, and if you further supplied or transferred any of the affected products to another facility or organization, let these facilities know of the recall and provide them with a copy of this notice. For questions, contact your local customer support representative,
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026