5.5MM Arthrogarde Hip Access Cannula
Reported: November 4, 2020 Initiated: September 21, 2020 #Z-0301-2021
Product Description
5.5MM Arthrogarde Hip Access Cannula
Reason for Recall
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.
Details
- Recalling Firm
- Smith & Nephew, Inc.
- Units Affected
- 143 units
- Distribution
- 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.
- Location
- Andover, MA
Frequently Asked Questions
What product was recalled? ▼
5.5MM Arthrogarde Hip Access Cannula. Recalled by Smith & Nephew, Inc.. Units affected: 143 units.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 4, 2020. Severity: Moderate. Recall number: Z-0301-2021.
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