Severity
Low
LowClass IIITerminated
FDA Devices recall · Reported September 21, 2016
VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated quantitative test for use on the instruments of the VIDAS family for the determination of N terminal fragment of Btype natriuretic peptide in human serum or plasma (lithium heparin) using the ELFA technique (EnzymeLinked Fluorescent Assay). The VIDAS NTproBNP (PBNP) test is used as an aid in the diagnosis of suspected congestive heart failure.
Due to a packaging error; The kit does not contain the correct number of C1 or C2 control vials.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Biomerieux France Chemin De L'Or recalled VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated quantitative t… - a low-severity action.
VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated quantitative t… was recalled by Biomerieux France Chemin De L'Or in September 21, 2016. Reason: Due to a packaging error; The kit does not contain the correct number of C1 or C2 control vials.. Check the official notice for the remedy. Verify recall #Z-2779-2016 with the FDA Devices before acting.
The recall
Biomerieux France Chemin De L'Or issued this low-severity FDA Devices recall-Due to a packaging error; The kit does not contain the correct number of C1 or C2 control vials..
- Low
- severity level
- Class III
- classification
- September 21, 2016
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2779-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2779-2016) was formally reported on September 21, 2016, with the manufacturer initiating the action on April 15, 2016. It is classified under Low severity (Class III), with a current status of Terminated. Biomerieux France Chemin De L'Or is listed as the recalling firm, operating out of Marcy L'Etoile, N/A. Federal records list the affected scope as 229 kits.
The documented reason for this recall is: Due to a packaging error; The kit does not contain the correct number of C1 or C2 control vials. Distribution data in the federal record shows the product reached: US Nationwide Distribution in the states of: AL, AZ, CA, FL, GA, IA, KS, KY, MA, MI, MN, NC, NE, NJ, NY, OH, SC, TX, VA and WV.. 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 low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
229 kits
Related Recalls
6
3 from same agency
Product description
VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated quantitative test for use on the instruments of the VIDAS family for the determination of N terminal fragment of Btype natriuretic peptide in human serum or plasma (lithium heparin) using the ELFA technique (EnzymeLinked Fluorescent Assay). The VIDAS NTproBNP (PBNP) test is used as an aid in the diagnosis of suspected congestive heart failure.
Reason for recall
Due to a packaging error; The kit does not contain the correct number of C1 or C2 control vials.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | Z-2779-2016 |
| Date reported | September 21, 2016 |
| Date initiated | April 15, 2016 |
| Recalling firm | Biomerieux France Chemin De L'Or |
| Firm location | Marcy L'Etoile, N/A |
| Affected scope | 229 kits |
| Distribution | US Nationwide Distribution in the states of: AL, AZ, CA, FL, GA, IA, KS, KY, MA, MI, MN, NC, NE, NJ, NY, OH, SC, TX, VA and WV. |
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-2779-2016) 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? ▼
VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated quantitative test for use on the instruments of the VIDAS family for the determination of N terminal fragment of Btype natriuretic peptide in human serum or plasma (lithium heparin) using the ELFA technique (EnzymeLinked Fluorescent Assay). The VIDAS NTproBNP (PBNP) test is used as an aid in the diagnosis of suspected congestive heart failure.. Recalled by Biomerieux France Chemin De L'Or. Units affected: 229 kits.
Why was this product recalled? ▼
Due to a packaging error; The kit does not contain the correct number of C1 or C2 control vials.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 21, 2016. Severity: Low. Recall number: Z-2779-2016.
Where was the recalled product distributed? ▼
Distribution: US Nationwide Distribution in the states of: AL, AZ, CA, FL, GA, IA, KS, KY, MA, MI, MN, NC, NE, NJ, NY, OH, SC, TX, VA and WV..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2779-2016) 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 September 21, 2016. 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.