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FDA DevicesClass III

Penner Pacific Bathing Spa, Model Numbers 860010-1L

Published: March 18, 2026Recall ID: Z-1508-2026Category: Medical DevicesCountry: United States
US
Medical DeviceFDA DevicesUSUS

Penner Pacific Bathing Spa, Model Numbers 860010-1L

Recalling Firm: Penner Patient Care, Inc.

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Reason for Recall / Hazard

The device does not bear a unique device identifier.

Product Description & Identification

Penner Pacific Bathing Spa, Model Numbers 860010-1L

Additional Source Details

FieldValue
CityAurora
StateNE
Event id98396
Address 1101 Grant St
Address 2N/A
Code infoUDI-DI: 0085007365409; Serial Numbers: 07246737902 10236603401 10226407101 03236488101 03246677601 08226379901 08226385601 12236632601 07226353601 08236572201 04246696501 01256844001 12246811601 06226337201 07236557301 09236582001 02246663101 09246761901 08226369401 08226374601 01246644601 04246691701 08246756001 10236600001 04256958001 04256952001
Postal code68818-3200
Report date20260318
Product typeDevices
Product quantity26 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 860010-1L?

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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Overview

  • Recalling FirmPenner Patient Care, Inc.
  • StatusOngoing
  • Risk LevelClass III
  • DistributionUS Nationwide distribution.
Recall Hazard Severity
High Alert (Class I)
Official Agency Alert

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🚨 SAFETY ALERT: Penner Patient Care, Inc. - Penner Pacific Bathing Spa, Model Numbers 860010-1L

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https://therecallfile.com/recalls/penner-pacific-bathing-spa-model-numbers-860010-1l/FDA-Z-1508-2026
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