Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ossur OB Resolve Recalled by Ossur Americas Due to Halo system products labeled MR conditional will undergo...
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 OB Resolve, Sterile, Part/ Description: 505300D/ OB RESOLVE STERILE RING SML; 505400D/ OB RESOLVE RING KIT STD; 505500D/ OB RESOLVE RING KIT LRG; 515300D/ OB RESOLVE RING KIT SM-No App; 515400D/ OB RESOLVE RING KIT STD-No App; 515500D/ OB RESOLVE RING KIT LG-No App; 540D/ OB RESOLVE COMPONENT TRAY
Quantity: 342
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
About Ossur Americas
Ossur Americas has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report