K31020151226AB — GovInfoNow

Take action

Contact the company & request your remedy

Recalling firmCommunity Products, LLC2032 Route 213 · Rifton, NY 12471

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

K31020151226AB

Why it’s dangerous

This is a low risk product. It is safe for general use.

Who’s affected

All

How to tell if you have this one

K31020151226AB

Brand
K31020151226AB
Category
Medical device

Based on the official FDA remedy

What to do — step by step

1
Check the product for any signs of damage or wear.
2
Ensure the product is used according to the manufacturer's instructions.

✎ GovInfoNow

Questions people ask

Is this product safe for general use?

Yes, this product is safe for general use.

What are the potential risks of using this product?

This product has a low risk level and is safe for general use.

Take action

Contact K31020151226AB

We’ve drafted a message you can send K31020151226AB to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1137-2026 — K31020151226AB K31020151226AB

Hello,

I own a K31020151226AB that is covered by recall Z-1137-2026 from K31020151226AB.

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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-1137-2026 (December 18, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1137-2026 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.

Community Products, LLC recalls Rifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM is a powered lift device for transferring clients in a

Lower-risk recall