Use cautionMedical device recall · FDA · Published November 20, 2018
Stryker Power-LOAD Cot Fastening System Model 6390 Recall: Broken Floor Plates Risk
Stryker recalls Power-LOAD Cot Fastening System Model 6390 (Catalog #6390-000-000) due to risk of broken floor plates during ambulance patient transport. Affected units have serial numbers listed in the recall notice.
The power load floor plates which hold the ambulance cot anchors in place during patient transport, may be broken.
Take action
Contact the company
📍Recalling firmStryker Medical Division of Stryker Corporation3800 E Centre Ave · Portage, MI 49002-5826
✎ GovInfoNow plain-language explainer
Stryker is recalling its Power-LOAD Cot Fastening System Model 6390 because the floor plates that hold ambulance cots in place may break during patient transport. This could lead to the cot becoming unstable and potentially causing injury to patients or medical staff. Read more at govinfonow.com/recall/69449-stryker-power-load-cot-fastening-system-model-6390-recall-broken.
“Stryker Power-LOAD Cot Fastening System Model 6390 Recall: Broken Floor Plates Risk.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/69449-stryker-power-load-cot-fastening-system-model-6390-recall-broken. Based on FDA recall #Z-1350-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1350-2019%22&limit=1).
The FDA has issued a Class II voluntary recall for Stryker Medical Division's Model 3009 ProCuity patient beds due to missing electrical safety test values, which present a risk of tissue burn or electrical shock.
How to tell if you have it
Stryker Medical Division
Model 3009 ProCuity
The hazard
Missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Context
Stryker Medical Division of Stryker Corporation has 17 other recalls on record since July 21, 2017. Recent related recalls include the Cub Pediatric Crib Model FL19H for missing warning labels and the Arise 1000EX Mattress for incompatible use with MV3 beds.
How to tell if you have this one
Check if your Power-LOAD Cot Fastening System has the model number 6390 and catalog number 6390-000-000. Affected units have serial numbers listed in the recall notice.
Brand
Stryker
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check for broken floor plates
Inspect the floor plates for cracks or damage that could cause them to break during patient transport.
Contact Stryker for replacement
If you find broken floor plates, contact Stryker directly for a replacement or repair.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “US Nationwide and the following foreign countries: Australia, Canada, Netherlands, South Africa, and Switzerland.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 20 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-1350-2019 (November 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1350-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 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.