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

Recall Z-0757-2024 — Maquet PowerLEDII OR Light System, Model Names and Catalog Numbers PWDII77SF - ARDPWT629100A, PWDII555DF - ARDPWT629101A, PWDII555SF - ARDPWT629102A, PWDII755DF - ARDPWT629103A, PWDII755SF - ARDPWT629104A, PWDII775DF - ARDPWT629105A, PWDII775SF - ARDPWT629106A, PWDII50DF - ARDPWT629109A, PWDII50SF -

U.S. FDA — Device Enforcement · United States · 2023-11-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0757-2024
Date of alert
2023-11-08
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Getinge Usa Sales Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
03700712414207
Reported risk: A potential for a light system to fall in the operating room.
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.