Home / Recalls / Merits Holdings Co. Dba Merits Health Products, Inc. / Z-1632-2020

Z-1632-2020 Class II Terminated

Recalled by Merits Holdings Co. Dba Merits Health Products, Inc. — Fort Myers, FL

FDA device recall Z-1632-2020 was initiated by Merits Holdings Co. Dba Merits Health Products, Inc. on Mar 2, 2020 and is designated Class II. Reason for recall: Pinion gear may disengage from track allowing lift to slip or jolt. The recall status is terminated (terminated Sep 18, 2023). Affected quantity: 82 units.

Recall details

Product Type: Devices
Report Date: Apr 8, 2020
Initiation Date: Mar 2, 2020
Termination Date: Sep 18, 2023
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 82 units.

Product description

Merits E604 Pilot Navigator Stairlift - Product Usage: To transport patients up stairs.

Reason for recall

Pinion gear may disengage from track allowing lift to slip or jolt.

Distribution pattern

US Nationwide distribution in the states of AZ, CA, CT, FL, GA, IN, MA, MD, ME, MO, NC, OH, PA, TX, and VA.

Code information

Model: E60424YLMUB; SN: MU180600588; (01) 04714379292589 (11)190604 (21) MU190600025.

Source

Dataset: openFDA device recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for Z-1632-2020
openFDA file date: Nov 10, 2026
Loaded by RegDataLab: Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.