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

Recall Z-1052-2019 — MultiDiagnost-Eleva, Product codes 708032, 708036 Product Usage: As a multifunctional I universal imaging application system, General RIF, Fluoroscopy, Radiography and Angiography can be performed along with more specialized interventional applications on human patients. This includes the follow

U.S. FDA — Device Enforcement · United States · 2019-02-28 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1052-2019
Date of alert: 2019-02-28
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Philips North America, LLC
Product category: device
Product type: Devices

Reported risk: The locking plate may be missing from the system, which may result in unexpected stand/table tilt movement that cannot be stopped by the user.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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.

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