Data Foundry

Medical device recalls 2020

Stryker Power-PRO TL cot-powered ambulance cot Model Number 6550 — Class II medical device recall Z-1935-2020

Terminated recall by Stryker Medical Division of Stryker Corporation, reported 2020-05-20. Ambulance Cots may not meet crash test standard BS EN 1789

Recall numberZ-1935-2020
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmStryker Medical Division of Stryker Corporation, Portage, MI, United States
Recall initiated2020-04-07
Classified2020-05-08
Reported by FDA2020-05-20
Terminated2021-01-22
Countries outside the USGB
Quantity34 units
UPC / GTIN / UDI-DI01909003700056, 01909003700070, 01909003700087
Serial numbers1909003700051, 1909003700052, 1909003700055, 1909003700056, 1909003700057, 1909003700058, 1909003700059, 1909003700060, 1909003700061, 1909003700062, 1909003700065, 1909003700066, 1909003700067, 1909003700068, 1909003700069, 1909003700070, 1909003700072, 1909003700073, 1909003700074, 1909003700075, 1909003700076, 1909003700077, 1909003700078, 1909003700079, 1909003700080 and 9 more
Model numbers6550

Product

Stryker Power-PRO TL cot-powered ambulance cot Model Number 6550 - Product Usage: is a powered wheeled stretcher that is intended to support and transport the entire body of a traumatized, ambulatory or non-ambulatory human patient (includes infants and adults).

Reason for recall

Ambulance Cots may not meet crash test standard BS EN 1789

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1935-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.