Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Ossur Recalled by Ossur Americas Due to Halo system products labeled MR conditional will undergo...

Date: June 21, 2018
Company: Ossur Americas
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Ossur Americas directly.

Affected Products

Ossur, J Tong, Sterile, Part/ Description: JT-115/ J TONG MED/LGE-No App; JT-200/ J TONG ASSEMBLY SML/MED; JT-210/ J TONG ONLY SML/MED; JT-400/ J TONG COMPONENT TRAY

Quantity: 138

Why Was This Recalled?

Halo system products labeled MR conditional will undergo confirmatory safety testing to confirm MR conditional parameters. In addition, the second line description on the titanium pin label mistakenly lists ceramic tip. The second line description should state titanium pin.

Where Was This Sold?

This product was distributed to 28 states: AL, AK, AZ, CA, DE, FL, GA, HI, IL, IN, KY, MA, MI, MN, MS, NE, NM, NY, NC, OH, PA, RI, SC, TN, TX, UT, VA, WA

Affected (28 states)Not affected

About Ossur Americas

Ossur Americas has 12 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report