Use cautionMedical device recall · FDA · Published April 7, 2020
Stryker Power-PRO TL Ambulance Cot May Not Meet Crash Test Standard
Stryker recalls Power-PRO TL ambulance cots (model 6550) that may not meet crash test standard BS EN 1789. Affected units include specific serial numbers listed in the recall notice.
“Stryker Power-PRO TL Ambulance Cot May Not Meet Crash Test Standard.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/65497-stryker-power-pro-tl-ambulance-cot-may-not-meet-crash. Based on FDA recall #Z-1935-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1935-2020%22&limit=1).
The FDA announced on April 7, 2020, that Stryker Medical Division of Stryker Corporation is voluntarily recalling Stryker Power-PRO TL cot-powered ambulance cots because they may not meet crash test standard BS EN 1789. The agency issued recall number Z-1935-2020 for the Class II device.
Stryker Power-PRO TL cot-powered ambulance cots may not meet crash test standard BS EN 1789. The powered wheeled stretchers are intended to support and transport the entire body of traumatized, ambulatory or non-ambulatory human patients.
Context
GovInfoNow's records show Stryker Medical Division of Stryker Corporation has had 17 other recalls on record since July 21, 2017. Other recent recalls of similar products include Stryker Cub Pediatric Crib Model FL19H Missing Warning Labels (Feb. 18, 2026), Stryker Arise 1000EX Mattress Recall: Incompatible Use with MV3 Beds (Oct. 31, 2025), and Stryker ProCuity Bed Model 3009: Risk of Tissue Burn or Electrical Shock (Aug. 30, 2023).
How to tell if you have this one
Check for the model number 6550 on the cot. Affected units have specific serial numbers listed in the recall notice, including 1909003700051 through 1909003700090.
Brand
Stryker
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Serial Numbers
Look for serial numbers 1909003700051 through 1909003700090 on the cot.
Contact Stryker
Reach out to Stryker for further assistance or to confirm if your unit is affected.
How this recall unfolded
Recall timeline
FDA terminated this recall 10 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1935-2020 (April 7, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1935-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.