PlainRecalls
CriticalClass IOngoing

FDA Drug recall · Reported March 11, 2026

MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7

Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil

Recall #
D-0397-2026
Affected scope
4
Initiated
December 15, 2025
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StuffbyNainax recalled MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7 - a critical-severity action.

MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7 was recalled by StuffbyNainax in March 11, 2026. Reason: Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadala…. Check the official notice for the remedy. Verify recall #D-0397-2026 with the FDA Drug before acting.

The recall

StuffbyNainax issued this critical-severity FDA Drug recall-Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadala….

Critical
severity level
4 units
affected scope
Class I
classification
March 11, 2026
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-0397-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) 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, 6 from FDA Drug - 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.

Drugs & Medications recalls over time

Where this recall sits in its category - 14,472 drugs & medications recalls on record

05001,0001,5002,000 2006201220152018202120242026 448
Severity1906864652High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified high severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7

Reason for recall

Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil

Recall Profile

Structured summary of the FDA Drug recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Critical (Class I)
Status Ongoing
Recall number D-0397-2026
Date reported March 11, 2026
Date initiated December 15, 2025
Recalling firm StuffbyNainax
Firm location Huntsville, TX
Affected scope 4
Distribution Product was distributed to 4 customers in the US.

Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

4 units affected - limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units) -
Large-scale (100K – 1M units) -
Massive (≥1M units) -

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (D-0397-2026) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Drug before acting, recall details can be updated.
  • This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next

This page summarizes the official FDA Drug 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?
MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7. Recalled by StuffbyNainax. Units affected: 4.
Why was this product recalled?
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil
Which agency issued this recall?
This recall was issued by the FDA Drug on March 11, 2026. Severity: Critical. Recall number: D-0397-2026.
Where was the recalled product distributed?
Distribution: Product was distributed to 4 customers in the US..
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.

Nationwide recalls with similar severity or category timing

Drug and device notices outside this firm and state, matched by severity timing and product category.

Compare this recall with Kian Pee Wan Capsules, 30-count bottles → · All Drugs & Medications recalls

This recall: FDA Drug, reported March 11, 2026. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026