Smith & Nephew SL PLUS MIA Adapter Recall: Pin Could Disassemble

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Recalling firmSmith & Nephew, Inc.1450 E Brooks Rd · Memphis, TN 38116-1804

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Smith & Nephew is recalling a specific surgical adapter because a pin might disassemble, potentially causing injury during use. Owners should check their lot numbers to see if they're affected.

Why it’s dangerous

The pin holding the spring mechanism isn't properly mounted. If it disassembles, it could cause injury during surgical procedures or equipment handling.

Who’s affected

Surgical professionals and medical facilities using the SL PLUS MIA DOUBLE OFFSET ADAPTER RIGHT 60/25MM. Those with lot numbers C63165, C63306, or C63495 are most at risk.

How to tell if you have this one

Check the product label for the lot numbers: C63165, C63306, or C63495. The product is the SL PLUS MIA DOUBLE OFFSET ADAPTER RIGHT 60/25MM with S&N 75004613.

Brand
Smith & Nephew
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Lot Number
Look for lot numbers C63165, C63306, or C63495 on the adapter's label.

✎ GovInfoNow

Questions people ask

Is this product dangerous if used properly?

The recall states the pin could disassemble, but it doesn't specify if the product is safe when used correctly.

What should I do if I have this product?

The recall record doesn't state a remedy, so no action is required unless you have the specific lot numbers listed.

How can I tell if my adapter is affected?

Check the lot number on the adapter's label; affected units have lot numbers C63165, C63306, or C63495.

Take action

Contact Smith & Nephew

We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0730-2019 — Smith & Nephew Smith & Nephew

Hello,

I own a Smith & Nephew that is covered by recall Z-0730-2019 from Smith & Nephew.

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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Where this comes from

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.

Official source: FDA Recall #Z-0730-2019 (January 7, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0730-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Smith & Nephew, Inc. recalls SL PLUS MIA DOUBLE OFFSET ADAPTER RIGHT 60/25MM, S&N 75004613

Use caution until it’s fixed