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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 74922

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
June 29, 2016
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Winco Mfg., LLC

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 3

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.

Z-0064-2017
Recall number
Z-0064-2017
Initiated
June 29, 2016
Classification
Class II
Status
Terminated
Recalling firm
Winco Mfg., LLC
Quantity
264 Stretcher Chairs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Non-conforming component caused arms of TMM4 Stretcher chair to no longer meet design specifications.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

All identified serial numbers.

Distribution pattern

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.

device · product 2 of 3

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.

Z-0065-2017
Recall number
Z-0065-2017
Initiated
June 29, 2016
Classification
Class II
Status
Terminated
Recalling firm
Winco Mfg., LLC
Quantity
264 Stretcher Chairs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Non-conforming component caused arms of TMM4 Stretcher chair to no longer meet design specifications.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

All identified serial numbers.

Distribution pattern

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.

device · product 3 of 3

TransMotion Medical, TMM5 Series Mobile Surgical 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.

Z-0066-2017
Recall number
Z-0066-2017
Initiated
June 29, 2016
Classification
Class II
Status
Terminated
Recalling firm
Winco Mfg., LLC
Quantity
264 Stretcher Chairs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Non-conforming component caused arms of TMM4 Stretcher chair to no longer meet design specifications.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

All identified serial numbers.

Distribution pattern

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.