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Smith & Nephew, Inc. recalls 5.5MM Arthrogarde Hip Access Cannula
Recalled November 4, 2020 · FDA recall Z-0301-2021 · Smith & Nephew
Hazard
The J Lock feature on the cannula body was manufactured incorrectly, preventing the cannula from locking into an irrigation extender or arthroscope in the correct orientation. · FDA Class II
Units
143 units
Sold at
Domestic Distribution: CA, CO, CT, GA, IA, IL, IN, MD, MO, NC, NY, OH, PA, SC, TN, TX, WA, WI, WV. International Distribution: AU, BR, CA, CL, CN, CO, DE, ES, GB, HK, KR, PA, PT, TW.
Description
The J Lock feature on the cannula body was manufactured incorrectly, preventing the cannula from locking into an irrigation extender or arthroscope in the correct orientation.
Product
5.5MM Arthrogarde Hip Access Cannula
Manufacturer(s)
Smith & Nephew, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →