MooreMedical Supporting Health & Care — Class II medical device recall Z-0910-2014
Terminated recall by Nipro Diagnostics, Inc., reported 2014-02-12, distributed nationwide. Manufactured with an incorrect factory set unit of measure.
| Recall number | Z-0910-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Nipro Diagnostics, Inc., Ft Lauderdale, FL, United States |
| Recall initiated | 2013-10-02 |
| Classified | 2014-02-03 |
| Reported by FDA | 2014-02-12 |
| Terminated | 2016-01-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BD, CA, IN, JM, PK, TH, TR, TT, VN |
| Quantity | 105 |
| Lot numbers | KK0964, KL01213, KL01233-3TI, KL0267-10, KL0381-14, KL0637-2TI, KL0716TI, KL0860TI, KP0074TI |
Product
MooreMedical Supporting Health & Care...MooreBrand Blood Glucose Monitor for Self-Testing & Multi-Patient Use TRUEtrack. Manufactured by: NIPRO DIAGNOSTICS, Fort Lauderdale, FL 33309 U.S.A. Is intended for the quantitative determination of glucose in human whole blood taken from finger or forearm.
Reason for recall
Manufactured with an incorrect factory set unit of measure.
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-0910-2014. 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.