Accueil/Tous les Rappels/FDA-Z-1235-2026
FDA DevicesClass II

CellMek SPS Sample Preparation System, REF: C44603, with software

Publié le: 11 février 2026ID du rappel: Z-1235-2026Catégorie: Dispositifs MédicauxPays: États-Unis
US
Medical DeviceFDA DevicesUSUS

CellMek SPS Sample Preparation System, REF: C44603, with software

Recalling Firm: Beckman Coulter, Inc.

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

Motif du rappel / Danger

Sample preparation system designed to automate staining, lysing, cell washing has a software error that causes samples to be dispensed close to or touching tube bottoms, which could dislodge fluid line, result in sample loss, spillage, make instrument inoperable and will lead to unintentional removal of 60-100 microliters from final sample, may lead to incorrect diagnosis or patient management.

Description du produit & Identification

CellMek SPS Sample Preparation System, REF: C44603, with software

Additional Source Details

FieldValue
CityMiami
StateFL
Event id98207
Address 111800 Sw 147th Ave
Address 2N/A
Code infoUDI-DI: 15099590750312. Software Version 2.3.90.0
Postal code33196-2500
Report date20260211
Product typeDevices
Product quantity50
Reason for recallSample preparation system designed to automate staining, lysing, cell washing has a software error that causes samples to be dispensed close to or touching tube bottoms, which could dislodge fluid line, result in sample loss, spillage, make instrument inoperable and will lead to unintentional removal of 60-100 microliters from final sample, may lead to incorrect diagnosis or patient management.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20251223
Initial firm notificationLetter
Center classification date20260202

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 CellMek SPS Sample Preparation System, REF: C44603, with software?

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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Aperçu

  • Entreprise responsableBeckman Coulter, Inc.
  • StatusOngoing
  • Niveau de risqueClass II
  • DistributionWorldwide - US Nationwide distribution in the states of MO, WA, MA, IL, AL, OR, IL and the countries of AB, BE, ES, FR, NL, ON, DE, AT, VIC, AU, GB, SK, MX, CH.
Recall Hazard Severity
High Alert (Class I)
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🚨 SAFETY ALERT: Beckman Coulter, Inc. - CellMek SPS Sample Preparation System, REF: C44603, with software

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https://therecallfile.com/fr/recalls/cellmek-sps-sample-preparation-system-ref-c44603-with-software/FDA-Z-1235-2026
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