Drugs & medicalClass II

Trackx Technology Inc recalls TrackX Insight Base Modular Instrument Tracker, 5L, REF #604-3TX, Sterile; and TrackX Insight Base Modular Instrument Tracker, 6.5L, Model…

The device is breaking and falling off the Nuvasive T-Handle with Hudson Adapter on certain Nuvasive XLIF instruments during surgery when malleted.

Read the official notice →
Date
2023-02-15
Country
United States
Brand
Trackx Technology
Product
TrackX Insight Base Modular Instrument Tracker, 5L, REF #604-3TX, Sterile; and TrackX Insight Base Modular Instrument Tracker, 6.5L, Model…
Classification
Class II
Units
US Nationwide distribution in the states of AZ, FL, LA, NC, PA, VA, WA, WI.
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Trackx Technology recalls

  1. 2024-11-06
  2. US
    Drugs & medicalClass III

    Trackx Technology Inc recalls Product Name: Insight Base Flex - 8, Ref 608-3TX; The device consists of a sterile Snap that includes reflective features that facilitate…

    The patient label stickers may have the wrong expiration date recorded. The contract manufacturer entered the manufacturing date (2024-04-01) as the expiration date. The actual expiration date of the product is…

    FDA · DeviceTrackx Technology IncNC, VA, FL, PA, NYOfficial notice →
All 2 Trackx Technology recalls →

Other drugs & medical recalls in the United States

  1. 2023-02-22
  2. US
    Drugs & medicalClass II

    Amerisource Health Services LLC recalls Metoprolol Succinate Extended-Release Tablets, USP, 50 mg, packaged in (a) 100-count bottle, NDC 68001-501-00; (b) 500-count…

    Failed Dissolution Specifications: This recall is being initiated in support of the recall by the manufacturer which included lots that were packaged for BluePoint Laboratories.

    FDA · DrugAmerisource Health Services LLCNationwide USAOfficial notice →
  3. US
    Drugs & medicalClass II

    McGuff Compounding Pharmacy Services, Inc. recalls Thiamine Hydrochloride 200 mg/2mL (100mg/mL), Riboflavin 2 mg/2mL (1mg/mL) Injection, FOR INTRAMUSCULAR OR SLOW…

    Presence of Particulate Matter: Presence of foreign substances were reported in vials at the pharmacy.

    FDA · DrugMcGuff Compounding Pharmacy Services, Inc.Nationwide in the USAOfficial notice →
  4. 2023-02-15
  5. US
    Drugs & medicalClass II

    Bard Peripheral Vascular Inc recalls The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a nitinol stent…

    An increase in the reported complaint rate for inability to deploy was identified and related to poor slide block bonding.

    FDA · DeviceBard Peripheral Vascular IncWorldwide - U.S. Nationwide distribution including in the states of AK, AL,…Official notice →
  6. US
    Drugs & medicalClass II

    Roche Molecular Systems, Inc. recalls cobas SARS-CoV-2 & Influenza A/B Qualitative nucleic acid test for use on the cobas 5800/6800/8800 Systems; Material Number…

    The firm received customer complaints regarding false negative Influenza A (Flu A) results and late Flu A Target Ct values. A false negative influenza A result may lead to additional testing, psychological distress,…

    FDA · DeviceRoche Molecular Systems, Inc.Domestic distribution nationwide. Foreign distribution worldwide.Official notice →
  7. US
    Drugs & medicalClass II

    Olympus Corporation of the Americas recalls SPiN Thoracic Navigation System Model: SYS-4000 (SYS-4000D)

    A grainy image is observed when using a SPiN Vision Single-Use Flexible Bronchoscope (models INS-7100 or INS-7130) with the SYS-4000 system due to an incorrect DVI cable supplied may result in prolonged…

    FDA · DeviceOlympus Corporation of the AmericasFL, GA, IN, MD, MS, NY, OH, PA, RI, SC, VAOfficial notice →
  8. US
    Drugs & medicalClass II

    Wishbone Medical, Inc. recalls WishBone Medical Smart Correction Dual Joint Express Struts, external skeleton fixation device Type Part Number XXS 10-702-080095-0 XS…

    Firm identified that user may be unable to adjust the length of the Smart Correction Dual Joint Express Struts due to the collar release pin backing out. This may lead to a delay in correction.

    FDA · DeviceWishbone Medical, Inc.US Nationwide distribution in the state of South Carolina.Official notice →
See all drugs & medical recalls →