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

Recall Z-0011-2015 — Nemschooff, Model Numbers - Serenity II:790-12, Serenity III: 791-12, Serenity III Exam: 791-12E, and Serenity IIS: 792-12. Designed to provide patient comfort during patient treatment sessions. The chair may include a manual control reclining mechanism. Customer configurable models are also availa

U.S. FDA — Device Enforcement · United States · 2011-01-18 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0011-2015
Date of alert: 2011-01-18
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Nemschoff Chairs, Inc.
Product category: device
Product type: Devices

Reported risk: Nemschoff Chairs, Inc. is recalling various model of the Serenity Treatment Chair because of potential elevated temperatures in the seat and back lumbar areas of the chair.

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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