ClearanceBrief
Recall Z-0740-2022 ยท HWC Screw, Fixation, Bone

Nextremity Solutions

Nextra Cannulated Hammertoe Standard Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toe SKU: CH-STD-KT

DateJan 13, 2022
StatusTerminated
ReasonDuring insertion of the middle phalanx implant into bone, the driver may deform the implant locking mechanism and result in inadequate mating force between the middle and proximal phalanx implants, resulting in surgical delay, in-situ removal of the implant, use of alternative surgical approach, disassembly of the implants post-operatively, and revision
Root causeDevice Design
ActionNextremity Solution issued URGENT Medical Device Recall dated 1/13/22. Letter states reason for recall, health risk and action to take: 1. Review this notification and ensure that affected team members are aware of the contents. 2. Immediately locate and quarantine affected product (see Table 1 above) in your trunk stock inventory. 3. Immediately return all affected product from your trunk stock inventory. a. Complete Attachment 1- Medical Device Recall Return Response and send to QA@nextremity.com within three (3) days. This form must be returned even if you do not have affected products ava
Quantity24 units
DistributionUS Nationwide distribution in the states of AZ, IL, GA, LA, MD, NY, PA, TX, WA.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K200840DuoHex CH Cannulated Hammertoe System
Nextremity Solutions, Inc., Jun 26, 2020
K213530Nextra CH Cannulated Hammertoe System
Nextremity Solutions, Inc., Dec 9, 2021