Recall Atlas
Drugs & medicalClass II

FlexDex Inc. recalls 8mm FlexDex Needle Driver, Product Code FD-335 ND

The firm is reinforcing the IFU instructions: "Do not use if the package is damaged." If upon inspection of the packaging, any damage is observed, including pinholes or tears in the pouch, the product should not be used.

Read the official notice →
Date
2022-02-02
Country
United States
Brand
FlexDex Inc.
Product
8mm FlexDex Needle Driver, Product Code FD-335 ND
Classification
Class II
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2022-02-09
  2. US
    Drugs & medicalClass II

    Ultra Seal Corporation recalls Pain & Sinus Reliever Pain Reliever/Nasal Decongestant (acetaminophen 500mg, Phenylephrine HCl 5mg) 2 tablet packets, Mfg for Advanced…

    cGMP deviations

    FDA · DrugUltra Seal CorporationNationwide within the United StatesOfficial notice →
  3. US
    Drugs & medicalClass II

    Ideal Specialty Apothecary, Inc. dba Ideal Pharmacy recalls Medroxyprogesterone Acetate Injection, IM, 150 mg/mL, packaged in 1 ml Single Dose Vial, RX Only, Ideal…

    Lack of Assurance of Sterility

    FDA · DrugIdeal Specialty Apothecary, Inc. dba Ideal Pharmacynationwide in the USAOfficial notice →
  4. US
    Drugs & medicalClass II

    Teva Pharmaceuticals USA recalls Doxylamine Succinate and Pyridoxine Hydrochloride Delayed-Release Tablets 10 mg/10 mg, 100-count bottle, Rx Only, Manufactured by:…

    Failed Dissolution Specification: Dissolution results are below specification limits for the active ingredient

    FDA · DrugTeva Pharmaceuticals USANationwide in the USAOfficial notice →
  5. 2022-02-02
  6. US
    Drugs & medicalClass II

    NuVasive Specialized Orthopedics, Inc. recalls MAGEC 1 System

    Safety Alert to all surgeons informing them of post-implantation fractures of an internal metallic component for device manufactured prior to March 26, 2015.

    FDA · DeviceNuVasive Specialized Orthopedics, Inc.WorldwideOfficial notice →
  7. US
    Drugs & medicalClass II

    Velano Vascular recalls PIVO Blood Collection Device 20G, REF: 202-0005

    Incomplete sealing of blood collection device unit packages may produce a breach in the sterile barrier enclosing the product. This could lead to microbial contamination of the device prior to use. The health effects…

    FDA · DeviceVelano VascularUS Nationwide distribution in the states of CT, CO, UT, PA, IL, WA, CA, NJ,…Official notice →
  8. US
    Drugs & medicalClass II

    NRT X-RAY A/S recalls 1. Footrest ( use exclusively in combination with Intelli-C devices) 2. Shoulder support ( use exclusively in combination with Intelli-C…

    Friction rubber block in the clamping mechanism was missing in the Footrest. It may slip down along the patient table while in use with a patient. This accessory is designed to use with Intelli-C, Right and Intelli-C,…

    FDA · DeviceNRT X-RAY A/SUSA: IA, KY,LA, MA, NC,NY, OH, SC, WA, WV OUS: Switzerland, Czech Republic,…Official notice →
See all drugs & medical recalls →