Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported August 13, 2014
AdvanDx Quick FISH Fixation Kit for BC ( Blood Cultures), 50 tests. In vitro diagnostic. The QuickFISH Fixation Kits are components that are sold separately for the Staphylococcus QuickFISH BC test Catalog number: QFFixBC1-50 (a component for QFSTABC1-50)
Positive result in the Internal negative control well for the Staphylococcus QuickFISH BC test, failing QC
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Advandx Inc recalled AdvanDx Quick FISH Fixation Kit for BC ( Blood Cultures), 50 tests. In vitro diagnostic. … - a moderate-severity action.
AdvanDx Quick FISH Fixation Kit for BC ( Blood Cultures), 50 tests. In vitro diagnostic. … was recalled by Advandx Inc in August 13, 2014. Reason: Positive result in the Internal negative control well for the Staphylococcus QuickFISH BC test, failing QC. Check the official notice for the remedy. Verify recall #Z-2138-2014 with the FDA Devices before acting.
The recall
Advandx Inc issued this moderate-severity FDA Devices recall-Positive result in the Internal negative control well for the Staphylococcus QuickFISH BC test, failing QC.
- Moderate
- severity level
- Class II
- classification
- August 13, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2138-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2138-2014) was formally reported on August 13, 2014, with the manufacturer initiating the action on July 4, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Advandx Inc is listed as the recalling firm, operating out of Woburn, MA. Federal records list the affected scope as 10 kits.
The documented reason for this recall is: Positive result in the Internal negative control well for the Staphylococcus QuickFISH BC test, failing QC Distribution data in the federal record shows the product reached: Distributed in the states of AZ, ID, FL, MO, OH, MI, NJ, and VA.. 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
10 kits
Related Recalls
6
3 from same agency
Product description
AdvanDx Quick FISH Fixation Kit for BC ( Blood Cultures), 50 tests. In vitro diagnostic. The QuickFISH Fixation Kits are components that are sold separately for the Staphylococcus QuickFISH BC test Catalog number: QFFixBC1-50 (a component for QFSTABC1-50)
Reason for recall
Positive result in the Internal negative control well for the Staphylococcus QuickFISH BC test, failing QC
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2138-2014 |
| Date reported | August 13, 2014 |
| Date initiated | July 4, 2014 |
| Recalling firm | Advandx Inc |
| Firm location | Woburn, MA |
| Affected scope | 10 kits |
| Distribution | Distributed in the states of AZ, ID, FL, MO, OH, MI, NJ, and VA. |
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-2138-2014) 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? ▼
AdvanDx Quick FISH Fixation Kit for BC ( Blood Cultures), 50 tests. In vitro diagnostic. The QuickFISH Fixation Kits are components that are sold separately for the Staphylococcus QuickFISH BC test Catalog number: QFFixBC1-50 (a component for QFSTABC1-50). Recalled by Advandx Inc. Units affected: 10 kits.
Why was this product recalled? ▼
Positive result in the Internal negative control well for the Staphylococcus QuickFISH BC test, failing QC
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 13, 2014. Severity: Moderate. Recall number: Z-2138-2014.
Where was the recalled product distributed? ▼
Distribution: Distributed in the states of AZ, ID, FL, MO, OH, MI, NJ, and VA..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2138-2014) 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 August 13, 2014. 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.