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Use caution Medical device recall · FDA · Published August 18, 2026

Charlotte Claw Screw Recall: Missing Threads Risk Surgery Complications

Wright Medical Technology recalls 34 Charlotte Claw Screws (Lot 1826666) distributed August 2025-April 2026. Missing threads may cause surgery delays or alternative procedures.

🇺🇸 FDA recall #Z-3334-2026Medical deviceWright Medical Technology ›
✎ GovInfoNow plain-language explainer

Wright Medical Technology recalls 34 Charlotte Claw Screws (Lot 1826666) that were manufactured with missing threads. This could prevent secure attachment to the plate during foot surgery, potentially requiring additional procedures or alternative surgeries. Read more at govinfonow.com/recall/1449351-wright-medical-technology-inc-recalls-charlotte-claw-screw-ref-40122716.

Source Summary by GovInfoNow · govinfonow.com/recall/1449351-wright-medical-technology-inc-recalls-charlotte-claw-screw-ref-40122716 · Updated October 14, 2026 · FDA enforcement record: FDA #Z-3334-2026

Cite this page

“Charlotte Claw Screw Recall: Missing Threads Risk Surgery Complications.” GovInfoNow, updated October 14, 2026. https://govinfonow.com/recall/1449351-wright-medical-technology-inc-recalls-charlotte-claw-screw-ref-40122716. Based on FDA recall #Z-3334-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3334-2026%22&limit=1).

The FDA announced on 2026-08-18 that Wright Medical Technology, Inc. is recalling the CHARLOTTE CLAW Screw (REF: 40122716) due to missing threads on screwheads. This defect may prevent secure engagement with plating systems, potentially prolonging surgery or requiring alternative methods.

How to tell if you have it

  • Brand: Wright Medical Technology
  • Product: CHARLOTTE CLAW Screw
  • REF: 40122716
  • UDI-DI: 00840420109705
  • Lot: 1826666
  • Distribution dates: 18-Aug-2025 through 09-Apr-2026
  • Units affected: 34

The hazard

According to the FDA, the screws were manufactured with missing threads on the screwheads. If used, this defect prevents a secure rigid engagement with the plate's internal threads, which may lead to surgery prolongation or the need for an alternative surgery method if no replacement device is readily available.

Context

GovInfoNow's records show Wright Medical Technology, Inc. has 20 other recalls on record since 2018-03-14. Other recent recalls include the 2024-03-06 Stryker Infinity Resection Adjustment Block Recall and the 2023-06-13 Stryker Infinity Alignment Frame Distal Sub-Assembly Recall. Similar product recalls in early 2026 include the 2026-02-25 Synthes 2.4V TAP CORTEX SCREW Recall and the 2026-03-16 Smith & Nephew TRIGEN Humeral Nail Recall.

How to tell if you have this one

Check for the screw model 'Charlotte Claw' with reference number 40122716. The lot number is 1826666, distributed from August 18, 2025, through April 9, 2026.

  • Brand
    Wright Medical Technology
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Your Screws

    Look for the reference number 40122716 and lot number 1826666 on the screws.

Where it went and when

Where it was distributed

Distributed nationwide; the notice names 11 states.

Alaska: nationwideAKMaine: nationwideMEVermont: nationwideVTNew Hampshire: nationwideNHWashington: nationwideWAIdaho: named in the noticeIDMontana: nationwideMTNorth Dakota: nationwideNDMinnesota: nationwideMNIllinois: nationwideILWisconsin: named in the noticeWIMichigan: named in the noticeMINew York: nationwideNYRhode Island: nationwideRIMassachusetts: nationwideMAOregon: nationwideORNevada: nationwideNVWyoming: nationwideWYSouth Dakota: nationwideSDIowa: nationwideIAIndiana: nationwideINOhio: nationwideOHPennsylvania: named in the noticePANew Jersey: named in the noticeNJConnecticut: nationwideCTCalifornia: named in the noticeCAUtah: nationwideUTColorado: named in the noticeCONebraska: nationwideNEMissouri: nationwideMOKentucky: nationwideKYWest Virginia: nationwideWVVirginia: nationwideVAMaryland: nationwideMDDelaware: nationwideDEArizona: nationwideAZNew Mexico: nationwideNMKansas: nationwideKSArkansas: nationwideARTennessee: named in the noticeTNNorth Carolina: nationwideNCSouth Carolina: nationwideSCDistrict of Columbia: nationwideDCOklahoma: named in the noticeOKLouisiana: nationwideLAMississippi: nationwideMSAlabama: nationwideALGeorgia: nationwideGAHawaii: nationwideHITexas: named in the noticeTXFlorida: named in the noticeFL

FDA distribution: “US Nationwide distribution in the states of FL, TX, PA, CA, ID, MI, OK, TN, NJ, WI, CO.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: California, Colorado, Florida, Idaho, Michigan, New Jersey, Oklahoma, Pennsylvania, Tennessee, Texas, Wisconsin.

Recall timeline

FDA published this recall 50 days after the firm started it.

1. Firm started the recall: Aug 18, 202612. FDA classified it Class II: Sep 30, 202623. Published in FDA’s Enforcement Report: Oct 7, 202634. Added to GovInfoNow: Oct 13, 202642026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-3334-2026 (August 18, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3334-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on October 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA