Merits E604 Pilot Navigator Stairlift - Product Usage: To… recallZ-1632-2020 · Merits Holdings Co. dba Merits Health Products, Inc. · initiated Mar 2, 2020
Terminated
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Merits Holdings Co. dba Merits Health Products, Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Pinion gear may disengage from track allowing lift to slip or jolt.
FDA root cause category: Device Design
What the company is doing
Merits Health Products notified customers on 03/17/2020 via "Medical Device Field Correction E604 Pilot Navigator" letter. The letter identified the affected product and requested the customers to complete the form.
Recall details
- Recall number
- Z-1632-2020
- Status
- Terminated
- Initiated by the company
- Mar 2, 2020
- Recalling firm
- Merits Holdings Co. dba Merits Health Products, Inc.
- Quantity
- 82 units.
- Product code
- KNO
- Distribution
- US Nationwide distribution in the states of AZ, CA, CT, FL, GA, IN, MA, MD, ME, MO, NC, OH, PA, TX, and VA.
Product description
Merits E604 Pilot Navigator Stairlift - Product Usage: To transport patients up stairs.
Code information (models, lots, serial numbers)
Model: E60424YLMUB; SN: MU180600588; (01) 04714379292589 (11)190604 (21) MU190600025.
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- MERITS E60424YLMUBMerits Health Products CO., Ltd. · Transport, Patient, Powered1 recall0 reports
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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