Drugs & medicalClass II

Wright Medical Technology, Inc. recalls stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation

Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.

Read the official notice →
Date
2023-05-03
Country
United States
Brand
Wright Medical Technology
Product
stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation
Classification
Class II
Units
US Nationwide distribution.
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Wright Medical Technology recalls

  1. 2026-10-07
  2. US
    Drugs & medicalClass II

    Wright Medical Technology, Inc. recalls CHARLOTTE CLAW Screw, REF: 40122716, intended for use with CLAW II Polyaxial Compression Plating System

    Screws, intended for use with polyaxial compression plating system intended for foot osteotomies, was manufactured with missing threads on the screwheads, which if used would prevent a secure rigid engagement with the…

    FDA · DeviceWright Medical Technology, Inc.US Nationwide distribution in the states of FL, TX, PA, CA, ID, MI, OK, TN,…Official notice →
  3. 2024-04-10
  4. US
    Drugs & medicalClass II

    Wright Medical Technology, Inc. recalls stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty

    Stryker has identified an issue that impacts specific lots of Infinity" Resection Guide Adjustment Blocks. The parts within these three lots were found to have been missing an internal screw in the finished instrument…

    FDA · DeviceWright Medical Technology, Inc.US: TX, NE, and AUSTRALIA, BELGIUM, BRAZIL, CANADA, CHINA, COLOMBIA, FRANCE,…Official notice →
  5. 2023-07-12
  6. US
    Drugs & medicalClass II

    Wright Medical Technology, Inc. recalls Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile.

    The devices were manufactured with the pin sleeve holes too narrow, which does not allow the pin sleeves to pass through the pin sleeve holes, thereby preventing pin placement through the pin holes.

    FDA · DeviceWright Medical Technology, Inc.There was no U.S. distribution, including government and military. Foreign…Official notice →
  7. 2023-03-08
  8. US
    Drugs & medicalClass II

    Wright Medical Technology, Inc. recalls ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 40241425, Bone fixation device

    Stryker has identified an issue that impacts two specific lots of CLAW" II plates. The plates within these two lots were found to have been comingled, resulting in the incorrect product in packages. Packaging for…

    FDA · DeviceWright Medical Technology, Inc.US Nationwide distribution in the state of NY.Official notice →
  9. 2022-11-02
  10. US
    Drugs & medicalClass II

    Wright Medical Technology, Inc. recalls Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3

    The tibial tray lock detail is oversized (larger than specification).

    FDA · DeviceWright Medical Technology, Inc.US Nationwide distribution in the state of New York.Official notice →
  11. 2022-10-12
  12. US
    Drugs & medicalClass II

    Wright Medical Technology, Inc. recalls stryker EVOLVE, Proline Stem, CoCr, Size: +4, OD: 9.5mm, REF 496S275, Wright s EVOLVE Proline Plus Radial Head and Repair System…

    The outer label does not match the device inside the package. The affected lot of EVOLVE Proline Stem 7.5mm +2 contains a size 9.5mm +4 stem, while the affected lot of EVOLVE Proline Stem 9.5mm +4 contains a size 7.5mm…

    FDA · DeviceWright Medical Technology, Inc.US Nationwide distribution.Official notice →
All 16 Wright Medical Technology recalls →

Other drugs & medical recalls in the United States

  1. 2023-05-03
  2. US
    Drugs & medicalClass II

    FUJIFILM Healthcare Americas Corporation recalls FujiFilm FDR AQRO (Model DR-XD1000)- A digital mobile X-ray system intended for use in general purpose radiography for…

    Arm which holds the tube head in place is susceptible to breaking, if the device breaks it could potentially cause serious harm or injury to the patient and/or user.

    FDA · DeviceFUJIFILM Healthcare Americas CorporationUS Nationwide distribution.Official notice →
  3. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls ARTIS one with a hybrid cable- An angiography system developed for diagnostic imaging and interventional procedures. Material…

    Examination room monitor connected with the hybrid cable may have a display issue and no image function is available

    FDA · DeviceSiemens Medical Solutions USA, IncWorldwide - US Nationwide distribution in the states of FL, SD, PR and the…Official notice →
  4. US
    Drugs & medicalClass II

    Mani, Inc. - Kiyohara Facility recalls Mani Trocar Kit, Model MTK23S and Model MTK25S There are 3 kits contained in one box, and sterile 1 kit consists of 3 pcs. trocar…

    A packaging defect may compromise the sterile barrier.

    FDA · DeviceMani, Inc. - Kiyohara FacilityDistribution in US - 1 consignee in MissouriOfficial notice →
  5. US
    Drugs & medicalClass II

    Covidien LP recalls VersaOne Reusable Positioning Cannula 11mm Standard, Model Number RC11STS

    There is a manufacturing non-conformance that may result in a metal shaving (burr) on the inside of the VersaOneTM Reusable Positioning Cannula, located where the Cannula and Body components are welded together.

    FDA · DeviceCovidien LPWorldwide - US Nationwide distribution in the states of NC and the countries…Official notice →
  6. US
    Drugs & medicalClass II

    Datascope Corp. recalls MAQUET CARDIOSAVE hybrid Intra-Aortic Balloon Pump, Model Number 0998-XX-0800-32

    The power cord supplied (Type J plug end) for the Cardiosave Hybrid IABP to Brazil is incompatible with the Brazilian Type N power receptacle.

    FDA · DeviceDatascope Corp.International distribution in the country of Brazil.Official notice →
  7. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls GEM NEUROTUBE, Absorbable Woven Polyglycolic Acid Mesh Tube, Product Codes: a) 5311-01240-010, b) 5311-01240-012; for peripheral…

    The product is brittle and potentially crumbling upon handling or when being removed from its package.

    FDA · DeviceBaxter Healthcare CorporationWorldwide distribution - US Nationwide and the countries of China, Germany,…Official notice →
See all drugs & medical recalls →