CLASS II Device recall · Reported 19 Oct 2016 · FDA Enforcement Report

TransMotion Medical, TMM3 Series Video-Fluoroscopy Swallow recalled

Winco Mfg is recalling TransMotion Medical, TMM3 Series Video-Fluoroscopy Swallow Study Stretcher-Chair, distributed in 29 states. The recall was initiated on 29 Jun 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll identified serial numbers.

Quantity recalled264 Stretcher Chairs

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-0064-2017
FDA event ID: 74922
Recalling firm: Winco Mfg, Ocala, FL
Classification: Class II
Status: Terminated
Recall initiated: 29 Jun 2016
FDA classified: 9 Oct 2016
Reported: 19 Oct 2016
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Imaging Equipment

Timeline

29 Jun 2016	Recall initiated by company
9 Oct 2016	Classified by FDA	+102 days
19 Oct 2016	Published in enforcement report	+10 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

TransMotion Medical, TMM3 Series Video-Fluoroscopy Swallow Study Stretcher-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.

Where it was distributed

Worldwide Distribution -- USA, including AR, CA, CO, CT, FL, GA, IL, KS, LA, MD, MI, MN, MO, MS, NC, NJ, NM, NV, NY, OH, OK, PA, RI, TN, TX, VA, WA, WI, and Puerto Rico; and the countries of Canada, Australia, Italy, Panama, Switzerland and Taiwan.

Arkansas California Colorado Connecticut Florida Georgia Illinois Kansas Louisiana Maryland Michigan Minnesota Missouri Mississippi North Carolina New Jersey New Mexico Nevada New York Ohio

Stores named: WinCo

Questions about this recall

Why was it recalled?

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

Which lots are affected?

All identified serial numbers.

Where was it sold?

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

2 other products · FDA event 74922

Reported	Class	Recall	Company	Reason	Where
19 Oct 2016	CLASS II	TransMotion Medical, TMM4 Series Multi-Purpose Treatment Chair recalled	Winco Mfg	Other	29 states
19 Oct 2016	CLASS II	TransMotion Medical, TMM5 Series Mobile Surgical Stretcher -Chair recalled	Winco Mfg	Other	29 states

More recalls from Winco Mfg

All 26

Reported	Class	Recall	Company	Reason	Where
19 Oct 2016Device	CLASS II	TransMotion Medical, TMM5 Series Mobile Surgical Stretcher -Chair recalled	Winco Mfg	Other	29 states
19 Oct 2016Device	CLASS II	TransMotion Medical, TMM4 Series Multi-Purpose Treatment Chair recalled	Winco Mfg	Other	29 states
26 Aug 2015Device	CLASS II	Winco Designer Care Cliner - with Nylon Casters Oncology recalled	Winco Mfg	Other	Nationwide
26 Aug 2015Device	CLASS II	Winco Elite Care Cliner w/Swing Away Arms X-Large recalled by Winco Mfg	Winco Mfg	Other	Nationwide
26 Aug 2015Device	CLASS II	Winco Drop Arm Care Cliner X-Large recalled by Winco Mfg	Winco Mfg	Other	Nationwide

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