FDA Medical Device Recalls (openFDA)
Nobel Biocare: Nobel Biocare N1 TiUltra TCC NP 3.5x13mm
- Recall number
- Z-1565-2022
- Recalling firm
- Nobel Biocare
- Product
- Nobel Biocare N1 TiUltra TCC NP 3.5x13mm
- Status
- Open, Classified
- Initiated
- 2022-07-25
- Posted
- 2022-08-23
- Terminated
- not on file
- Reason
- Due to the presence of a burr which may cause an aspiration risk to patient during surgical procedure.
- Root cause
- Process change control
- 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 us.cs.complaints@nobelbiocare.com 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.
- Quantity
- 347 devices
- Distribution
- 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
- Lot, serial or model codes
- Catalog number: 300859 Lot numbers / UDI Codes: 12167337 / (01)07332747161717(10)12167337(11)210119(17)251218 12167830 / (01)07332747161717(10)12167830(11)210125(17)251224 12168184 / (01)07332747161717(10)12168184(11)210128(17)251227
- 510(k) numbers
- K211109
- PMA numbers
- not on file
- Product code
- DZE
- Firm FEI
- 3002807692
- Firm city
- Goteborg
- Firm state
- not on file
- Firm country
- Sweden
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28