PlainRecalls

Nextremity Solutions

15 recalls on record · Latest: Apr 20, 2022

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Agency notice ledger

Federal filing book Nextremity Solutions LIGHT-BOOK · SINGLE-AGENCY

#1,042 of 14,151 · 15 notices · 0.014% archive

  • BOOK 15 notices
  • RANK #1,042 of 14,151
  • SHARE 0.014% archive
  • AGENCY FDA Devices (15)
  • CAT medical devices
  • CATS 1 category
  • LATEST Apr 20, 2022
  • PHOTO Acumed LLC

Nearest notice-volume peer: Acumed LLC (0 notice gap)

Nextremity Solutions accounts for about 0.014% of the 104,423-notice archive on 15 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Nextremity Solutions's standing among 14,151 recalling firms

Nextremity Solutions ranks 1,042nd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Nextremity Solutions vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

15 1042nd of 14151 higher than 13,088 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-14

Nextremity Solutions in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Nextremity Solutions holds about 0.014% of archive notices alongside 15 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Apr 20, 2022

Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Cut SKU: NX-3532K-SC Orthopedic surgical instrument

FDA Devices Moderate Apr 20, 2022

Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical instrument

FDA Devices Moderate Apr 20, 2022

Nextra Hammertoe Correction System 3.5 Middle 3.2 Proximal Kit SKU: NX-3532K Orthopedic surgical instrument

FDA Devices Moderate Apr 20, 2022

Nextra Hammertoe Correction System 4.5 Middle 3.2 Proximal Kit SKU: NX-4532K Orthopedic surgical instrument

FDA Devices Moderate Apr 20, 2022

Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Cut SKU: NX-4532K-SC Orthopedic surgical instrument

FDA Devices Moderate Mar 16, 2022

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

FDA Devices Moderate Mar 16, 2022

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

FDA Devices Moderate May 5, 2021

InCore Lapidus Disposable Kit 28mm Left, Part Number: IC-LAP-28L - Product Usage: Intended as a three-part construct intended for internal fixation for First Metatarsocuneiform arthrodesis.

FDA Devices Moderate May 5, 2021

InCore Lapidus Disposable Kit 28mm Right, Part Number: IC-LAP-28R - Product Usage: Intended as a three-part construct intended for internal fixation for First Metatarsocuneiform arthrodesis.

FDA Devices Moderate Mar 18, 2020

Nextra Hammertoe Correction System-4.5MM Middle, 3.2MM Proximal, SS, Sterile. REF: NX-4532K - Product Usage: The Nextra Hammertoe Correction System is a system of implants and associated instruments which is indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toes.

FDA Devices Moderate Feb 19, 2020

Stratum Lapidus Plate - Small Rt, Part No. STRM-LAP-SMR, UDI 00817701025467. The product is part of the Stratum Foot Plating System, a plate and screws construction indicated for bone fixation.

FDA Devices Moderate Jan 15, 2020

Stratum MDS Screw 3.5x50mm ST Part Number: STRM-MDS-3550ST

FDA Devices Moderate Jan 15, 2020

Stratum MDS Screw 3.5x46mm ST Part Number: STRM-MDS-3546ST

FDA Devices Moderate Jan 15, 2020

Stratum MDS Screw 3.5x48mm ST Part Number: STRM-MDS-3548ST

FDA Devices Moderate Dec 4, 2019

Stratum Foot Plating System-NL LP Screw 3.5x50mm ST, sterile. Catalog Number: STRM-NL-3550ST - Product Usage: The Stratum Foot Plating System is a plate and screws construct indicated for fixation of fractures, osteotomies, nonunions, malunions and fusions of small bones and small bone segments, particularly in osteopenic bone.

Nextremity Solutions holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Frequently Asked Questions

How many federal recall notices name Nextremity Solutions?
PlainRecalls indexes 15 distinct federal recall events naming Nextremity Solutions, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Nextremity Solutions sit among other recalling firms?
Nextremity Solutions ranks #1,042 of 14,151 by distinct recall-event count among 14,151 firms in this archive (92nd percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Nextremity Solutions's notices?
FDA Devices accounts for 15 of this firm's 15 indexed notices.
What product category dominates Nextremity Solutions's filing book?
Filings for Nextremity Solutions span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous?
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Nextremity Solutions: 15 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Nextremity Solutions; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026