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FDA DevicesClass II

Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3

Published: August 5, 2026Recall ID: Z-2795-2026Category: Medical DevicesCountry: United States
US
Medical DeviceFDA DevicesUSUS

Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3

Recalling Firm: Permobil Inc

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Reason for Recall / Hazard

This recall has been reported retroactively. The power wheelchair firmware lacks a speed restriction to maintain stability when the seat lift exceeds 50 mm, which may cause the user to fall from the wheelchair or the wheelchair to tip over,

Product Description & Identification

Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3

Affected Products

Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3

Additional Source Details

FieldValue
CityLebanon
StateTN
Event id99315
Address 1300 Duke Dr
Address 2N/A
Code infoAll Units operating with firmware version 1.26.2/UDI:(01)17330818345674
Postal code37090-8115
Report date20260805
Product typeDevices
Product quantity140 units
Reason for recallThis recall has been reported retroactively. The power wheelchair firmware lacks a speed restriction to maintain stability when the seat lift exceeds 50 mm, which may cause the user to fall from the wheelchair or the wheelchair to tip over,
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20240229
Initial firm notificationLetter
Center classification date20260724

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 Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3?

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 FirmPermobil Inc
  • StatusOngoing
  • Risk LevelClass II
  • DistributionWorldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KY, ME, MI, MN, MO, MS, MT, NC, ND, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, WV, WY and the country of CAN.
Recall Hazard Severity
High Alert (Class I)
Official Agency Alert

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🚨 SAFETY ALERT: Permobil Inc - Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3

Check if your household is affected:
https://therecallfile.com/recalls/permobil-m3-corpus-power-wheelchair-with-heavy-duty-shock-ref-120031-m/FDA-Z-2795-2026
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