Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported April 24, 2013
Duane Reade TRUEtrack monitor kit, UPC# 6 39194 01679 7 Part # A4006-81 The TRUEtrack Blood Glucose System is intended for the quantitative determination of glucose in human whole blood taken from finger or forearm. The System is intended to be used to assist the patient and healthcare professional in the management of diabetes.
Meter kit outer boxes containing 10 ct. test strips state incorrect storage temperature range.
Nipro Diagnostics, Inc. recalled Duane Reade TRUEtrack monitor kit, UPC# 6 39194 01679 7 Part # A4006-81 The TRUEtrack … - a moderate-severity action.
Duane Reade TRUEtrack monitor kit, UPC# 6 39194 01679 7 Part # A4006-81 The TRUEtrack … was recalled by Nipro Diagnostics, Inc. in April 24, 2013. Reason: Meter kit outer boxes containing 10 ct. test strips state incorrect storage temperature range.. Check the official notice for the remedy. Verify recall #Z-1140-2013 with the FDA Devices before acting.
The recall
Nipro Diagnostics, Inc. issued this moderate-severity FDA Devices recall-Meter kit outer boxes containing 10 ct. test strips state incorrect storage temperature range..
- Moderate
- severity level
- Class II
- classification
- April 24, 2013
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1140-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1140-2013) was formally reported on April 24, 2013, with the manufacturer initiating the action on February 25, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Nipro Diagnostics, Inc. is listed as the recalling firm, operating out of Ft Lauderdale, FL. Federal records list the affected scope as 1,627 Kits.
The documented reason for this recall is: Meter kit outer boxes containing 10 ct. test strips state incorrect storage temperature range. Distribution data in the federal record shows the product reached: Nationwide Distribution only in NY.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
1,627 Kits
Related Recalls
6
3 from same agency
Product description
Duane Reade TRUEtrack monitor kit, UPC# 6 39194 01679 7 Part # A4006-81 The TRUEtrack Blood Glucose System is intended for the quantitative determination of glucose in human whole blood taken from finger or forearm. The System is intended to be used to assist the patient and healthcare professional in the management of diabetes.
Reason for recall
Meter kit outer boxes containing 10 ct. test strips state incorrect storage temperature range.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1140-2013 |
| Date reported | April 24, 2013 |
| Date initiated | February 25, 2013 |
| Recalling firm | Nipro Diagnostics, Inc. |
| Firm location | Ft Lauderdale, FL |
| Affected scope | 1,627 Kits |
| Distribution | Nationwide Distribution only in NY. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-1140-2013) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Duane Reade TRUEtrack monitor kit, UPC# 6 39194 01679 7 Part # A4006-81 The TRUEtrack Blood Glucose System is intended for the quantitative determination of glucose in human whole blood taken from finger or forearm. The System is intended to be used to assist the patient and healthcare professional in the management of diabetes.. Recalled by Nipro Diagnostics, Inc.. Units affected: 1,627 Kits.
Why was this product recalled? ▼
Meter kit outer boxes containing 10 ct. test strips state incorrect storage temperature range.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 24, 2013. Severity: Moderate. Recall number: Z-1140-2013.
Where was the recalled product distributed? ▼
Distribution: Nationwide Distribution only in NY..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1140-2013) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported April 24, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.