Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2130-2023 — Power-PRO 2- A powered ambulance cot that consists of a platform, including a mattress, mounted on a wheeled, retractable X-frame that is designed to support and transport a maximum weight of 700 lb (318 kg). Model Number: 6507

U.S. FDA — Device Enforcement · United States · 2023-05-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2130-2023
Date of alert
2023-05-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Stryker Medical Division of Stryker Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
650700000000
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.