Accueil/Tous les Rappels/FDA-Z-1501-2026
FDA DevicesClass III

Penner Pacific Bathing Spa, Model Numbers 360020-1EP

Publié le: 18 mars 2026ID du rappel: Z-1501-2026Catégorie: Dispositifs MédicauxPays: États-Unis
US
Medical DeviceFDA DevicesUSUS

Penner Pacific Bathing Spa, Model Numbers 360020-1EP

Recalling Firm: Penner Patient Care, Inc.

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

Motif du rappel / Danger

The device does not bear a unique device identifier.

Description du produit & Identification

Penner Pacific Bathing Spa, Model Numbers 360020-1EP

Additional Source Details

FieldValue
CityAurora
StateNE
Event id98396
Address 1101 Grant St
Address 2N/A
Code infoUDI-DI: 0085007365402; Serial Numbers: 03203147501 01192957001 06203171301 07203175701 11162597701 11193074801 11193074802 09193074801 09193074802 09193074803
Postal code68818-3200
Report date20260318
Product typeDevices
Product quantity10 units
Reason for recallThe device does not bear a unique device identifier.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20250813
Initial firm notificationLetter
Center classification date20260309

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 Devices).

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 Penner Pacific Bathing Spa, Model Numbers 360020-1EP?

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 Devices). 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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Outils gratuits

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Aperçu

  • Entreprise responsablePenner Patient Care, Inc.
  • StatusOngoing
  • Niveau de risqueClass III
  • DistributionUS Nationwide distribution.
Recall Hazard Severity
High Alert (Class I)
Alerte officielle de l’agence

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🚨 SAFETY ALERT: Penner Patient Care, Inc. - Penner Pacific Bathing Spa, Model Numbers 360020-1EP

Check if your household is affected:
https://therecallfile.com/fr/recalls/penner-pacific-bathing-spa-model-numbers-360020-1ep/FDA-Z-1501-2026
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