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

Recall Z-0287-2013 — PT Link Waterbath, Model#PT100. Lab Vision PT Module Plus provides an automated standarized alternative to labor intensive and time consuming dewaxing and epitote retrieval procedures.

U.S. FDA — Device Enforcement · United States · 2008-05-01 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0287-2013
Date of alert: 2008-05-01
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Dako North America Inc.
Product category: device
Product type: Devices

Reported risk: Dako is recalling the PT Link Waterbath because of a possible electrical hazard. Specifically, if the heater pad under the reagent tank becomes wet, it may present an electrical shock hazard when the lid is open.

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.

Recall Z-0287-2013 — PT Link Waterbath, Model#PT100. Lab Vision PT Module Plus provides an automated standarized alternative to labor intensive and time consuming dewaxing and epitote retrieval procedures.

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