CLASS II Device recall · Reported 20 Mar 2019 · FDA Enforcement Report
Ossur OB Resolve, Sterile, Part/ Description recalled by Ossur Americas
Ossur Americas is recalling Ossur OB Resolve, Sterile, Part/ Description: 505300D/ OB Resolve Sterile Ring Sml, distributed in 28 states. The recall was initiated on 21 Jun 2018 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0999-2019
- FDA event ID
- 80520
- Recalling firm
- Ossur Americas, Foothill Ranch, CA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 21 Jun 2018
- FDA classified
- 11 Mar 2019
- Reported
- 20 Mar 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Sterility
- Device type
- Medical Software
Timeline
| 21 Jun 2018 | Recall initiated by company | |
| 11 Mar 2019 | Classified by FDA | +263 days |
| 20 Mar 2019 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
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.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
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
Where it was distributed
U.S.: HI, AL, CA, WA, AZ, TX, NM, NE, MI, IL, MN, MS, IN, OH, KY, TN, AK, AL, UT, SC, NC, GA, PA, FL, NY, DE, RI, VA, MA; Foreign: Australia, Germany, New Zealand, Belgium
AlaskaAlabamaArizonaCaliforniaDelawareFloridaGeorgiaHawaiiIllinoisIndianaKentuckyMassachusettsMichiganMinnesotaMississippiNorth CarolinaNebraskaNew MexicoNew YorkOhio
Questions about this recall
Is Ossur OB Resolve, Sterile, Part/ Description: 505300D/ OB Resolve Sterile Ring Sml recalled?
Yes. Ossur Americas recalled Ossur OB Resolve, Sterile, Part/ Description: 505300D/ OB Resolve Sterile Ring Sml on 21 Jun 2018. The recall is Class II and its status is Terminated. Recall number Z-0999-2019.
Why was it 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.
Which lots are affected?
All lots of the products manufactured from 06/30/2009 - 12/13/2018
Where was it sold?
U.S.: HI, AL, CA, WA, AZ, TX, NM, NE, MI, IL, MN, MS, IN, OH, KY, TN, AK, AL, UT, SC, NC, GA, PA, FL, NY, DE, RI, VA, MA; Foreign: Australia, Germany, New Zealand, Belgium
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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