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Biologic Therapies, Inc recalls Bio-PLASTY Cannula (Needle)
Recalled April 8, 2015 · FDA recall Z-1372-2015 · Biologic Therapies
Hazard
Devices are misbranded - failure to properly classify and obtain FDA clearance prior distribution · FDA Class II
Units
58
Sold at
US Distribution in states of: MA, CA, WA, NJ, TX, IL, and FL.
Description
Devices are misbranded - failure to properly classify and obtain FDA clearance prior distribution
Product
Bio-PLASTY Cannula (Needle)
Manufacturer(s)
Biologic Therapies, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →