Smith & Nephew recalls 5.5MM Arthrogarde Hip Access Cannulas with faulty J Lock that may not lock correctly into irrigation extenders or arthroscopes during surgery.
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.
Smith & Nephew is recalling 5.5MM Arthrogarde Hip Access Cannulas because the J Lock feature was made incorrectly. This could prevent the cannula from locking into irrigation extenders or arthroscopes properly during surgery, potentially causing complications.
The J Lock feature was manufactured incorrectly, so the cannula may not lock into irrigation extenders or arthroscopes in the correct orientation. This could lead to improper use during hip surgery, potentially causing complications.
Surgical teams using the recalled cannulas for hip procedures are affected. Patients undergoing hip surgery with these cannulas may be at risk of improper use during the procedure.
Check for the model number 72201743 and lot numbers 50838788, 50834909, 50846565, 50842905, or 50822169 on the cannula packaging or label.
Look for model number 72201743 and lot numbers 50838788, 50834909, 50846565, 50842905, or 50822169 on the cannula packaging or label.
The J Lock feature was manufactured incorrectly, preventing the cannula from locking into irrigation extenders or arthroscopes in the correct orientation during hip surgery.
Check the model and lot numbers on the cannula packaging or label to see if it is recalled. If it is, contact Smith & Nephew for further instructions.
The recall record does not specify a remedy or fix for this issue.
We’ve drafted a message you can send Smith & Neph: Inc. to request your refund or repair — edit it as you like.
Subject: Recall Z-0301-2021 — Smith & Neph: Inc. Smith & Neph: Inc. Hello, I own a Smith & Neph: Inc. that is covered by recall Z-0301-2021 from Smith & Neph: Inc.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
