US Recall News

United States Recall News Alerts for Recalled Drugs, Food, Products, & Vehicles

MENUMENU
  • Home
  • About
    • Advertise
  • Full Recall News Archive
    • Top Story

      J&J Settles Talc Mesothelioma Settlement

      By Sandra Dalton, Staff Writer On January 6, 2020, Superior Court Judge Stephen Kaus announced that Johnson & Johnsons (J&J) had agreed to … [Read More...]

      Turkana Food Inc. Recall Flora Dried Apricots with Undeclared Sulfites on Product Labeling Because of Possible Health Risk

      Summary Company Announcement Date: June 12, 2025 FDA Publish Date: June … [Read More...]

    • More Safety Articles
    • Federal Preemption of State Product Liability Law
  • Drug Recalls
    • Abilify
    • Benicar
    • Fluoroquinolones
    • Invokana
    • Lipitor
    • Nuplazid
    • Opioids
    • OxyContin
    • Pradaxa
    • Proton Pump Inhibitors (PPIs)
    • Risperdal
    • SSRI
    • Symptoms & Side Effects
    • Taxotere
    • Testosterone
    • Uloric
    • Valsartan
    • Xarelto
    • Zofran
  • Medical Devices
    • 3M Earplug
    • 3T Heater-Cooler System
    • Bair Hugger
    • Bipolar Hip System
    • Essure
    • Hip Replacements
    • Implanon
    • IVC Filters
    • Hernia Mesh
    • Power Morcellators
    • Shoulder Implants
    • Transvaginal Mesh
  • Food Recalls
    • FDA Press Releases
    • USDA Press Releases
  • Auto Recalls
    • Air Bags
    • Ignitions
    • NHTSA Press Releases
    • Off-Road Utility Vehicles
    • Snowmobiles
    • Tires
  • Other Products
    • Asbestos
    • Baby Products
    • Pet Products
    • Roundup
    • Talcum Powder
    • Toy Recalls
You are here: Home / Urgent Recalls / Synthes USA, Ti Synex II Vertebral Body Replacement

Synthes USA, Ti Synex II Vertebral Body Replacement

November 13, 2009 By The FDA 2 Comments

Recall Class: Class I
Date Recall

Initiated:

September 14, 2009
Product:

Ti Synex II Vertebral Body Replacement (VBR)

 

This recall involves part numbers 04.808.001-11, Synex II Central Body, Titanium (all lots).

 

Part Numbers Descriptions

04.808.001

04.808.002

04.808.003

04.808.004

04.808.005

04.808.006

04.808.007

04.808.008

04.808.009

04.808.010

04.808.011

 

Ti Synex (TM) II Central Body 14 mm – 19 mm

Ti Synex (TM) II Central Body 17 mm – 25 mm

Ti Synex (TM) II Central Body 21 mm – 29 mm

Ti Synex (TM) II Central Body 25 mm – 33 mm

Ti Synex (TM) II Central Body 29 mm – 44 mm

Ti Synex (TM) II Central Body 37 mm – 52 mm

Ti Synex (TM) II Central Body 45 mm – 71 mm

Ti Synex (TM) II Central Body 58 mm – 84 mm

Ti Synex (TM) II Central Body 71 mm – 97 mm

Ti Synex (TM) II Central Body 84 mm -110 mm

Ti Synex (TM) II Central Body 97 mm -123 mm

 

This product was manufactured from June 8, 2007 through September 9, 2009 and distributed from July 2, 2007 through September 8, 2009.

Use: This device is a vertebral body replacement device that is used in the T1-L5 portion of the spine to replace a collapsed, damaged, or unstable vertebral body due to a tumor or trauma (that is, a fracture).
Recalling Firm: Synthes USA
1302 Wrights Lane East
West Chester, Pennsylvania  19380-3417
Reason for Recall: Loss of device height may result in nerve injury, increased pain, spinal compression fracture, failure of additional fixation, and/or need for a reoperation or an operation to modify the implanted device.
Public Contact:

Physicians who have:

  • questions may contact the company at 1-800-620-7025 extension 5375, 8:30 a.m. – 4:30 p.m., Monday through Friday, Eastern Time.
  • patients who experienced adverse reactions/events with this device should report to Synthes at:
    • Phone: 1-800-752-0128, 8:30 a.m.- 4:30 p.m., Monday through Friday, Eastern Time, or
    • Email:  ComplaintUnit@synthes.com

 

Patients who have this recalled device and have increased pain, other symptoms, or questions should contact their surgeon.

For more information, see Useful Links below.

 

FDA District: Philadelphia
FDA Comments:

Hospitals and surgeons that have these recalled devices must stop implanting them immediately.

On September 23, 2009, the company notified hospitals and sales consultants about this recall by mail.  The company:

  • identified the recalled product
  • described the problem and potential health effects
  • provided instructions to their customers to return all products in their inventory and all surgically removed devices for evaluation.
  • notified and provided instructions to physicians and patients (through their physicians)

On November 09, 2009, the company sent physicians a follow up letter for their patients.

Class 1 recalls are the most serious type of recall and involve situations in which there is a reasonable probability that use of these products will cause adverse health consequences or death.

Share this:

  • Click to share on Facebook (Opens in new window) Facebook
  • Click to share on X (Opens in new window) X
  • Click to share on LinkedIn (Opens in new window) LinkedIn
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

Related

Filed Under: Urgent Recalls

About The FDA

The Food and Drug Administration (FDA) is an agency within the U.S. Department of Health and Human Services. It consists of the Office of the Commissioner and four directorates overseeing the core functions of the agency: Medical Products and Tobacco, Foods and Veterinary Medicine, Global Regulatory Operations and Policy, and Operations.

Comments

  1. JUDITH L ROTONDO says

    June 25, 2010 at 12:02 am

    How do you truly know if your physician at that time of surgery used the recalled items or not?

    Reply
  2. Emily Neumann says

    August 17, 2010 at 2:47 pm

    I have this device and was notified of the recall. I am a year out of surgury and still have bad pain. I was told by my doctors NOT under any circumstances to contact my surgeon. No matter what my questions cant be answered because no one knows the answers. Its kind of hard when you feel all alone.

    Reply

Leave a ReplyCancel reply

This site uses Akismet to reduce spam. Learn how your comment data is processed.

Facebook
Thomas Roney LLC
Economic Consulting

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Turkana Food Inc. Recall Flora Dried Apricots with Undeclared Sulfites on Product Labeling Because of Possible Health Risk

June 12, 2025 By The FDA

Vita-Warehouse Corp. Issues Allergy Alert on Undeclared Peanut Allergen in ALDI Welby®, Berkley Jensen®, and VitaGlobe™ Vitamin B12 Gummy Products

June 12, 2025 By The FDA

Bugaboo North America Recalls Giraffe High Chairs Due to Risk of Serious Injury or Death from Fall Hazard

June 11, 2025 By The CPSC

Hero Highlight

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Mammut Sports Group Recalls Skywalker Pro Via Ferrata Sets Due to Risk of Serious Injury or Death from Fall Hazard

June 11, 2025 By The CPSC

Endless Pools Recalls Manual Retractable Pool Covers Due to Drowning and Entrapment Hazards; Risk of Serious Injury and Death

June 11, 2025 By The CPSC

TTI Outdoor Power Equipment Recalls RYOBI 40-Volt 24-Inch Cordless Hedge Trimmers Due to Laceration Hazard

June 11, 2025 By The CPSC

Medtronic Announces Voluntary Recall of Select Newport™ HT70 and Newport™ HT70 Plus Ventilators and Certain Related Newport™ Service Parts

June 11, 2025 By The FDA

Hofood99 Inc Recalls Enoki Mushroom Due to Possible Health Risk

June 11, 2025 By The FDA

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Medtronic Announces Voluntary Recall of Select Newport™ HT70 and Newport™ HT70 Plus Ventilators and Certain Related Newport™ Service Parts

June 11, 2025 By The FDA

Hofood99 Inc Recalls Enoki Mushroom Due to Possible Health Risk

June 11, 2025 By The FDA

Bornstein Seafoods Inc Recalls Cooked & Peeled Ready-To-Eat Coldwater Shrimp Meat Because of Possible Health Risk

June 10, 2025 By The FDA

Recall News in Your Inbox

Enter your email address to receive automated recall news updates.

Recent Comments

  • Roger McGowan on ABH NATURE’S PRODUCTS, INC, ABH PHARMA, INC., and STOCKNUTRA.COM, INC. Issues Nationwide Recall of All Lots of Dietary Supplement Products
  • Kathryn Moore on FDA Wants Cancer Warning on Breast Implants
  • BRAD on Huge ATV Recall by Polaris – Sportsman and Scrambler
  • Crystal Anderson on Allergan Voluntarily Recalls BIOCELL® Textured Breast Implants and Tissue Expanders
  • Outsourcing Training on The Modern Marketing of Pain
  • SANDRA Collett on Processed Food Preservative Linked to Autism?
  • Eric Karsh on Health Risks of Roundup Go Well Beyond Cancer

Recent Posts

  • Turkana Food Inc. Recall Flora Dried Apricots with Undeclared Sulfites on Product Labeling Because of Possible Health Risk
  • Vita-Warehouse Corp. Issues Allergy Alert on Undeclared Peanut Allergen in ALDI Welby®, Berkley Jensen®, and VitaGlobe™ Vitamin B12 Gummy Products
  • Bugaboo North America Recalls Giraffe High Chairs Due to Risk of Serious Injury or Death from Fall Hazard
  • Agro Superior Group Recalls Oliver & Smith Mattresses Due to Risk of Serious Injury or Death from Fire Hazard; Violation of Federal Standard for Mattress Flammability
  • More than One Million Anker Power Banks Recalled Due to Fire and Burn Hazards; Manufactured by Anker Innovations
  • Mammut Sports Group Recalls Skywalker Pro Via Ferrata Sets Due to Risk of Serious Injury or Death from Fall Hazard
  • Endless Pools Recalls Manual Retractable Pool Covers Due to Drowning and Entrapment Hazards; Risk of Serious Injury and Death
  • TTI Outdoor Power Equipment Recalls RYOBI 40-Volt 24-Inch Cordless Hedge Trimmers Due to Laceration Hazard
  • Medtronic Announces Voluntary Recall of Select Newport™ HT70 and Newport™ HT70 Plus Ventilators and Certain Related Newport™ Service Parts
-- See More Recall News

Disclaimer: The information contained in these topics is not intended nor implied to be a substitute for professional medical or legal advice, it is provided for educational purposes only. Always seek the advice of your physician or other qualified healthcare provider about any questions you may have regarding a medical condition. Nothing contained in these topics is intended to be used for medical diagnosis or treatment.


ATTORNEY ADVERTISING. The information provided on this website is not legal advice. No attorney-client relationship is formed by the use of this site. It is not stated or implied that a lawyer is certified as a specialist in any particular field of law. No results are guaranteed, and prior results do not guarantee a similar outcome. This site is informational, only, not dispositive; it is up to you to decide whether a particular lawyer is right for you. Use of this site is subject to your agreement to these.


Copyright © 2025 Altrumedia · Terms of Service · Log in