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

Recall Z-2162-2013 — Tempa DOT Single-Use Clinical Thermometer Medical Indicators Made in U.S.A. by Medical Indicators, Inc. 16 Thomas J Rhodes Industrial Drive, Hamilton, NJ 08619 USA Phone 1.888.737.1601 www.medicalindicators.com Per 3M website (this product line was recently bought by Medical Indicators from 3M

U.S. FDA — Device Enforcement · United States · 2013-07-10 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2162-2013
Date of alert: 2013-07-10
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Medical Indicators, Inc.
Product category: device
Product type: Devices

Reported risk: TempaDot products may have been mislabeled.

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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