Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming component caused arms of TMM4 Stretcher chair...

Date: June 29, 2016
Company: Winco Mfg., LLC
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Winco Mfg., LLC directly.

Affected Products

TransMotion Medical, TMM4 Series Multi-Purpose Treatment Chair. Intended use is to provide the caregiver a single platform for receiving, transporting within a facility, performing procedures, recovery and discharge of patients in a monitored outpatient environment.

Quantity: 264 Stretcher Chairs

Why Was This Recalled?

Non-conforming component caused arms of TMM4 Stretcher chair to no longer meet design specifications.

Where Was This Sold?

This product was distributed to 28 states: AR, CA, CO, CT, FL, GA, IL, KS, LA, MD, MI, MN, MS, MO, NV, NJ, NM, NY, NC, OH, OK, PA, RI, TN, TX, VA, WA, WI

Affected (28 states)Not affected

About Winco Mfg., LLC

Winco Mfg., LLC has 26 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report