Stryker Finger Joint Implant Recall: Incorrect Sizing Label on Packaging

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Recalling firmWright Medical Technology, Inc.1023 Cherry Rd · Memphis, TN 38117-5423

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Stryker is recalling finger joint implants with incorrect sizing labels on the carton packaging. This could lead to improper sizing if the label is mistaken for the actual size, but there is no immediate safety risk.

Why it’s dangerous

The carton packaging has an incorrect sizing label, which could lead to using the wrong size implant. This might cause improper fitting during surgery, but the hazard does not involve immediate safety risks like injury or death.

Who’s affected

Patients who received the specific implant model with lot numbers 1728375 or 1728376 are likely affected. Surgeons and medical staff using the product are at risk of mislabeling.

How to tell if you have this one

Check for the product name 'Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00' with lot numbers 1728375 or 1728376. The UDI number is 00840420121707.

Brand
Stryker
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for the lot numbers 1728375 or 1728376 on the carton packaging.

✎ GovInfoNow

Questions people ask

Is this product dangerous?

No, the recall is for labeling issues only and does not pose an immediate safety risk.

How do I know if I have the recalled product?

Check for the product name 'Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00' with lot numbers 1728375 or 1728376.

What should I do if I have the recalled product?

The recall does not require immediate action; check the label and contact Stryker for further guidance.

Take action

Contact Stryker

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

✉️ Open in email

Subject: Recall Z-1567-2022 — Stryker Stryker

Hello,

I own a Stryker that is covered by recall Z-1567-2022 from Stryker.

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-1567-2022 (July 27, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1567-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 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.

Wright Medical Technology, Inc. recalls Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.

Lower-risk recall