Tempa DOT Single-Use Clinical Thermometer Medical Indicators Made in U — Class II medical device recall Z-2162-2013
Terminated recall by Medical Indicators, Inc., reported 2013-09-18, distributed nationwide. TempaDot products may have been mislabeled.
| Recall number | Z-2162-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medical Indicators, Inc., Hamilton, NJ, United States |
| Recall initiated | 2013-07-10 |
| Classified | 2013-09-06 |
| Reported by FDA | 2013-09-18 |
| Terminated | 2014-01-16 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| Lot numbers | 06068, 06083, 06112, 06126, 06129, 06138, 06153, 06219, 06225 |
Product
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) and labeling in 806, TempaDOT thermometers are individually wrapped, single-use, disposable clinical thermometers for oral or axillary use.
Reason for recall
TempaDot products may have been mislabeled.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2162-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.