Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported November 26, 2025
Meridian Bioscience, Group B Streptococcus, Catalog Number 480050, Nucleic Acid Amplification Test Assay
The cap on the reaction buffer tube may be missing the black rubber gasket resulting in the potential for leakage and reduced buffer volume.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Meridian Bioscience Inc recalled Meridian Bioscience, Group B Streptococcus, Catalog Number 480050, Nucleic Acid Amplifica… - a moderate-severity action.
Meridian Bioscience, Group B Streptococcus, Catalog Number 480050, Nucleic Acid Amplifica… was recalled by Meridian Bioscience Inc in November 26, 2025. Reason: The cap on the reaction buffer tube may be missing the black rubber gasket resulting in the potential for lea…. Check the official notice for the remedy. Verify recall #Z-0569-2026 with the FDA Devices before acting.
The recall
Meridian Bioscience Inc issued this moderate-severity FDA Devices recall-The cap on the reaction buffer tube may be missing the black rubber gasket resulting in the potential for lea….
- Moderate
- severity level
- Class II
- classification
- November 26, 2025
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0569-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0569-2026) was formally reported on November 26, 2025, with the manufacturer initiating the action on October 7, 2025. It is classified under Moderate severity (Class II), with a current status of Ongoing. Meridian Bioscience Inc is listed as the recalling firm, operating out of Cincinnati, OH. Federal records list the affected scope as 109 in total.
The documented reason for this recall is: The cap on the reaction buffer tube may be missing the black rubber gasket resulting in the potential for leakage and reduced buffer volume. Distribution data in the federal record shows the product reached: US Distribution to states of: AL, CO, FL, GA, IL, MD, ME, MT, NH, NJ, OH, TN, TX and WA; and OUS (foreign) countries of: Canada, Italy, and Panama.. 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
109 in total
Related Recalls
6
3 from same agency
Product description
Meridian Bioscience, Group B Streptococcus, Catalog Number 480050, Nucleic Acid Amplification Test Assay
Reason for recall
The cap on the reaction buffer tube may be missing the black rubber gasket resulting in the potential for leakage and reduced buffer volume.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-0569-2026 |
| Date reported | November 26, 2025 |
| Date initiated | October 7, 2025 |
| Recalling firm | Meridian Bioscience Inc |
| Firm location | Cincinnati, OH |
| Affected scope | 109 in total |
| Distribution | US Distribution to states of: AL, CO, FL, GA, IL, MD, ME, MT, NH, NJ, OH, TN, TX and WA; and OUS (foreign) countries of: Canada, Italy, and Panama. |
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-0569-2026) 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? ▼
Meridian Bioscience, Group B Streptococcus, Catalog Number 480050, Nucleic Acid Amplification Test Assay. Recalled by Meridian Bioscience Inc. Units affected: 109 in total.
Why was this product recalled? ▼
The cap on the reaction buffer tube may be missing the black rubber gasket resulting in the potential for leakage and reduced buffer volume.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 26, 2025. Severity: Moderate. Recall number: Z-0569-2026.
Where was the recalled product distributed? ▼
Distribution: US Distribution to states of: AL, CO, FL, GA, IL, MD, ME, MT, NH, NJ, OH, TN, TX and WA; and OUS (foreign) countries of: Canada, Italy, and Panama..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0569-2026) 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 November 26, 2025. 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.