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Recall Observatory FDA recall evidence

Device product

OSTEOVATIONEX 3CC INJECT FORMULA. REF/UDI: 390-0003/00813845020016 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.

Z-2181-2020

April 02, 2020

Class II

Product summary

Firm
Osteomed, LLC
Event
Event 85529
Status
Terminated
Classification
Class II
Quantity
270
Official record key
device-enforcement:Z-2181-2020

Official wording

Reason: Incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration.

Code information: LOT 17100402, 1127942, 1130302, 1135740, 1142070, 1142943

Distribution pattern: Worldwide distribution - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA. MA, MD, ME. MI, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV and WY and the countries of AUSTRALIA, ITALY, KOREA, MALAYSIA, PERU, SINGAPORE and THAILAND.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration.