Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
activforce 2 package labeling: Model: Activ5-M R 201-200563 Recalled by Activbody, Inc. Due to Due to: 1) Manufacturing issue that result in...
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 Activbody, Inc. directly.
Affected Products
activforce 2 package labeling: Model: Activ5-M R 201-200563
Quantity: 145 kits in U.S.
Why Was This Recalled?
Due to: 1) Manufacturing issue that result in inaccurate force measurement which may lead to may potential lead to incorrect treatment planning. 2) Firm failing to register and list its medical devices with U.S. Food and Drug Administration.
Where Was This Sold?
This product was distributed to 43 states: AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, IL, IN, IA, KS, LA, ME, MD, MA, MI, MN, MS, MO, NV, NH, NJ, NM, NY, NC, OH, OR, PA, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, DC
About Activbody, Inc.
Activbody, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report