Med-Riser MR600 Patient Lift Recall: Risk of Boom Pivot Failure

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Recalling firmMed-Mizer, Inc.80 Commerce Dr, N/A · Batesville, IN 47006-6700

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Med-Mizer is recalling Med-Riser MR600 Patient Lifts with serial numbers from MR600000 to MR600240 because the boom pivot could become loose, potentially causing the lift to fail during use. This poses a risk of injury if the lift malfunctions while lifting patients.

Why it’s dangerous

The boom pivot on the lift can become loose due to the nut securing the boom becoming loose and the bolt not being securely attached to the flange on the side. If this happens, the lift could fail while in use, potentially causing injury to patients or caregivers.

Who’s affected

Patients and caregivers who own or use Med-Riser MR600 Patient Lifts with serial numbers from MR600000 to MR600240 are most at risk. Healthcare facilities using these lifts should check their inventory.

How to tell if you have this one

Check your Med-Riser MR600 Patient Lift for a serial number starting with MR600000 and ending with MR600240. The recall covers all units with these specific serial numbers.

Brand
Med-Mizer
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Serial Number
Look for the serial number on your Med-Riser MR600 Patient Lift, which starts with MR600000 and ends with MR600240.
Contact Manufacturer
Reach out to Med-Mizer, Inc. for further instructions on how to address the issue with your lift.

✎ GovInfoNow

Questions people ask

What is the specific hazard with the Med-Riser MR600 Patient Lift?

The boom pivot could become loose due to the nut securing the boom becoming loose and the bolt not being securely attached to the flange on the side, which may cause the lift to fail during use.

How can I tell if my Med-Riser MR600 Patient Lift is affected?

Your lift is affected if it has a serial number starting with MR600000 and ending with MR600240.

What should I do if my lift is affected?

Contact Med-Mizer, Inc. for instructions on how to address the issue with your lift.

Take action

Contact Med-Mizer

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

✉️ Open in email

Subject: Recall Z-1204-2023 — Med-Mizer Med-Mizer

Hello,

I own a Med-Mizer that is covered by recall Z-1204-2023 from Med-Mizer.

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-1204-2023 (February 3, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1204-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.

Med-Mizer, Inc. recalls Med-Riser MR600 Patient Lift

Use caution until it’s fixed