NOBEL BIOCARE SERVICES AG Balz-zimmermannstrasse 7 Kloten Switzerland NobelReplace Conical Connection (CC) PMC RP 4.3x10mm, REF: 37291 - Product Usage: implants are intended to be used in the upper or lower jaw bone (osseointegration) and used for anchoring or supporting tooth replacements to restore chewing function. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
NobelReplace Conical Connection (CC) PMC RP 4.3x10mm, REF: 37291 - Product Usage: implants are intended to be used in the upper or lower jaw bone (osseointegration) and used for anchoring or supporting tooth replacements to restore chewing function.
Brand
NOBEL BIOCARE SERVICES AG Balz-zimmermannstrasse 7 Kloten Switzerland
Lot Codes / Batch Numbers
Lot: 13084072, UDI: (01)07332747073584(10)13084072(17)240525
Products Sold
Lot: 13084072, UDI: (01)07332747073584(10)13084072(17)240525
NOBEL BIOCARE SERVICES AG Balz-zimmermannstrasse 7 Kloten Switzerland is recalling NobelReplace Conical Connection (CC) PMC RP 4.3x10mm, REF: 37291 - Product Usage: implants are inten due to Dental implant cap label may incorrectly indicate implant measurements 5.0x8mm. Actual implant measurements are 4.3x10mm. If not noticed prior to impl. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Dental implant cap label may incorrectly indicate implant measurements 5.0x8mm. Actual implant measurements are 4.3x10mm. If not noticed prior to implant placement, this could lead to: 1) A second surgical procedure; 2) Implant replacement; 3) If placed in posterior lower jaw, the implant may damage the inferior alveolar nerve canal or perforate a small artery requiring immediate implant removal.
Recommended Action
Per FDA guidance
On 07/20/20, Urgent Medical Device Recall notices were emailed to customers who were asked to do the following: 1. Inspect your stock and confirm that both the cap label and the vial label indicate 4.3x10mm. 2. Quarantine devices with cap label 5.0x8mm. 3. Complete attached Customer Acknowledgment Form, even if you do not have any affected stock, and return it to the recalling firm via email. 4. Return all incorrectly labeled devices to the firm. Correctly labeled devices do not need to be returned. 5. Ensure relevant staff members are informed of this recall. If you have supplied or transferred any potentially affected product to another facility or organization, let that facility know of the recall by providing a copy of this letter. 6. Firm will replace returned affected devices. If you require any further information or support, please contact your local customer support representative at 714-282-4800 ext. 1527.
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