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Open, Classified

Nobel Biocare N1 TiUltra TCC NP 3.5x13mm

FDA Recall Z-1565-2022 · Posted 2022-08-23

Recalling FirmNobel Biocare
Recall StatusOpen, Classified
Product CodeDZE
Date Initiated2022-07-25
Product Quantity347 devices

Reason for Recall

Due to the presence of a burr which may cause an aspiration risk to patient during surgical procedure.

Firm Action

On 07/25/2022, Nobel Biocare AB sent an "URGENT MEDICAL DEVICE RECALL" Letter via UPS to customers informing them that there may be a burr present on the co-packed OsseoShaper 1 around the waist of the device. The hazard is primarily identified as a risk of the patient swallowing or inhaling the burr if it comes loose from the OsseoShaper 1 during the clinical procedure. Customer are instructed to: 1. Inspect their stock and quarantine affected devices. 2. Complete attached Customer Acknowledgment Form, even if they do not have any affected stock, and return it to Nobel Biocare, via email to [email protected] or fax 714-282-5073 within 5 days of receipt of this notice. 3. Return all affected stock on hand to Nobel Biocare using the shipping label attached to this notice. 4. Ensure relevant staff members are informed of this recall. If they 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 notice. Nobel Biocare has implemented preventive actions and will replace devices subject to this recall free of charge. For questions - contact local customer support representative at 800-322-5001 ext. 1527.

Root Cause

Process change control

Distribution Pattern

U.S Nationwide.: AZ, CA, CT, FL, HI, NC, NY, OR, PA, TX, UT, and WI O.U.S.: Austria, Belgium, Canada, Germany, Spain, France, United Kingdom, Hungary, Iceland, Italy, Netherlands, Norway, Portugal, and Sweden

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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