SwishTapered Implant Recall: Incorrect Packaging May Cause Misuse

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Recalling firmImplant Direct Sybron Manufacturing, LLC3050 E Hillcrest Dr, N/A · Westlake Village, CA 91362-3171

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Implant Direct is recalling SwishTapered Implant products used in dental bridgework because the packaging might be upside down. This could cause improper use if the implant is not installed correctly.

Why it’s dangerous

The implant extender may be packaged upside down in the plastic retainer. This could lead to incorrect installation if the user doesn't check the packaging orientation before use.

Who’s affected

Dental patients who use SwishTapered Implant for fixed dental bridgework are likely affected. Patients with the specific part numbers and lots listed are at risk of improper installation.

How to tell if you have this one

Check the product label for part numbers 934106, 934112, 934806, 934812, 934814, or 935712. Also check the lot numbers listed for each part number.

Brand
Implant Direct
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Packaging Orientation
Ensure the implant extender is not upside down in the plastic retainer before use.

✎ GovInfoNow

Questions people ask

Is this recall for dental implants?

Yes, this recall is for SwishTapered Implant used in dental bridgework.

What part numbers are affected?

Affected part numbers include 934106, 934112, 934806, 934812, 934814, and 935712 with specific lot numbers.

Do I need to stop using the implant?

No, but you should check the packaging orientation before use to ensure it's not upside down.

Take action

Contact Implant Direct

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

✉️ Open in email

Subject: Recall Z-1167-2018 — Implant Direct Implant Direct

Hello,

I own a Implant Direct that is covered by recall Z-1167-2018 from Implant Direct.

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-1167-2018 (January 19, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1167-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 31, 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.

Implant Direct Sybron Manufacturing, LLC recalls SwishTapered Implant Intended for use in support for fixed bridgework.

Lower-risk recall