Stryker Power-PRO 2 Ambulance Cot Recall: Base Leg Assembly May Bend
Stryker recalls Power-PRO 2 ambulance cots with serial numbers from 2112001485 to 2211001651. The base leg assembly may bend, causing difficulty engaging/disengaging from fasteners and affecting loading/unloading from ambulances. Affected units shipped between February 2022 and February 2023.
Use caution until it’s fixed
Base leg assembly may bend and result in difficulty engaging/disengaging from fastener, difficulty loading/unloading from ambulance, difficulty raising or lowering the cot, cot tip, or erratic or unintended motion.
Contact the company
What happened, in plain English
Stryker is recalling Power-PRO 2 ambulance cots that may have a bent base leg assembly. This can cause problems with engaging/disengaging from fasteners and loading/unloading the cot from ambulances. The recall affects units shipped between February 2022 and February 2023. Read more at govinfonow.com/recall/58088-stryker-power-pro-2-ambulance-cot-recall-base-leg-assembly.
Source Summary by GovInfoNow · govinfonow.com/recall/58088-stryker-power-pro-2-ambulance-cot-recall-base-leg-assembly · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2130-2023
Cite this page
“Stryker Power-PRO 2 Ambulance Cot Recall: Base Leg Assembly May Bend.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/58088-stryker-power-pro-2-ambulance-cot-recall-base-leg-assembly. Based on FDA recall #Z-2130-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2130-2023%22&limit=1).
Why it’s dangerous
The base leg assembly may bend, making it difficult to engage/disengage from fasteners and causing issues with loading/unloading the cot from ambulances. This could lead to improper handling or instability during use.
Who’s affected
Ambulance crews and medical personnel who use the Power-PRO 2 cots are most at risk. Units shipped between February 2022 and February 2023 are affected.
How to tell if you have this one
Check for serial numbers listed in the recall: 2112001485 to 2211001651. Units shipped between February 11, 2022 and February 1, 2023 are affected.
- Brand
Stryker- Category
Medical device
What to do — step by step
Check Your Serial Number
Look for the serial number on your Power-PRO 2 ambulance cot. If it matches the list of affected serial numbers (2112001485 to 2211001651), it is part of the recall.
Contact Stryker
If your cot is affected, contact Stryker directly to arrange for a replacement or repair.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Worldwide distribution - US Nationwide and the countries of Australia, Canada, Netherlands, Switzerland, United Kingdom.” 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 published this recall 56 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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-2130-2023 (May 24, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2130-2023 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.