Z-1026-2022Class II

Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The kit includes...

Name: Z-1026-2022 Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The kit includes...
Creator: restor3d Inc.
Published: 2022-03-30
License: https://open.fda.gov/license/

restor3d, Inc. / initiated 2022-03-30 / Terminated / root cause: labeling and UDI

FDA source

restor3d Inc. began a recall of Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The kit includes 3 trials. Orthopedic manual surgical instrument on 2022-03-30. FDA classified it as Class II and gives the reason as "Product labeled incorrectly. The lot was labeled with Small footprint when the product was Medium". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as labeling and UDI.

Recall record

Recall number: Z-1026-2022
Classification: Class II
Status: Terminated
Initiated: 2022-03-30
Posted: 2022-04-29
Terminated: 2023-08-28
Recalling firm: restor3d, Inc.
Product: Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The kit includes 3 trials. Orthopedic manual surgical instrument
Product code: LXH Orthopedic Manual Surgical Instrument
Reason for recall: Product labeled incorrectly. The lot was labeled with Small footprint when the product was Medium.
Root cause tag: labeling and UDI
FDA root cause: Process change control
Action: An email was sent out to the consignees on 03/31/2022. All customers were instructed to segregate any affected product and contact Restor3d. If all product has already been returned to restor3d, the consignee is to indicate that on the enclosed response form. On 04/19/2022, the firm extended the recall to two additional lots. The recall notification was sent to the consignees via email with a request for all affected product to be returned.
Quantity in commerce: 14 units
Distribution: US Nationwide distribution in the states of KY, NC, NJ, TX, IN, VA and AL.
Product codes and lots: Model: 6110-N01-KTS01 Lot: 2022030005 UDI: 00840097504506

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1026-2022
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1026-2022	Class II	Terminated	Voluntary: Firm initiated	2022-05-11	2022-04-29
Z-1027-2022	Class II	Terminated	Voluntary: Firm initiated	2022-05-11	2022-04-29
Z-1028-2022	Class II	Terminated	Voluntary: Firm initiated	2022-05-11	2022-04-29

Product code LXH

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)