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.
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.
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.
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.
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.
Check for serial numbers listed in the recall: 2112001485 to 2211001651. Units shipped between February 11, 2022 and February 1, 2023 are affected.
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.
If your cot is affected, contact Stryker directly to arrange for a replacement or repair.
Stryker is recalling Power-PRO 2 ambulance cots with serial numbers from 2112001485 to 2211001651 due to potential base leg assembly bending.
Contact Stryker directly to arrange for a replacement or repair.
The affected cots were shipped between February 11, 2022 and February 1, 2023.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2130-2023 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2130-2023 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
