Accueil/Tous les Rappels/FDA-D-0397-2026
FDA DrugsClass I

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

Publié le: 11 mars 2026ID du rappel: D-0397-2026Catégorie: Médicaments & SantéPays: États-Unis
US
PharmaceuticalFDA DrugsUSUS

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

Recalling Firm: StuffbyNainax

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Traduire l’alerteTranslate notice text, hazard warnings, and descriptions into any supported language.

Motif du rappel / Danger

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

Description du produit & Identification

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

Additional Source Details

FieldValue
CityHuntsville
StateTX
Event id98256
Address 12830 Lake Rd Apt 1102
Address 2N/A
Code infoAll codes; Exp 12/31/2029
Postal code77340-5662
Report date20260311
Product typeDrugs
Product quantity4
Reason for recallMarketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20251215
Initial firm notificationPress Release
Center classification date20260318

Consumer Action Protocol: What You Should Do Immediately

Safety Steps
1Verify Product Identifiers

Inspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.

2Isolate & Discontinue Use

Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.

3Claim Free Statutory Remedy

Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.

4Report Adverse Incidents

If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (FDA Drugs).

Your Legal Rights as a Consumer

Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.

Frequently Asked Questions About This Recall

FAQ Guide

Q1:What should I do immediately if I own or bought MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7?

Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.

Q2:Can I get a full refund or free repair for this recall?

Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.

Q3:Do I need my original sales receipt to claim a remedy or refund?

In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.

Q4:Where can I verify official information for this safety alert?

This safety alert is aggregated directly from official regulatory agency records (FDA Drugs). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.

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Aperçu

  • Entreprise responsableStuffbyNainax
  • StatusOngoing
  • Niveau de risqueClass I
  • DistributionProduct was distributed to 4 customers in the US.
Recall Hazard Severity
High Alert (Class I)
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🚨 SAFETY ALERT: StuffbyNainax - MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7

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https://therecallfile.com/fr/recalls/mr-7-super-700000-capsules-1-capsule-blister-card-distributed-by-mr-7/FDA-D-0397-2026
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