Startseite/Alle Rückrufe/FDA-Z-1093-2026
FDA DevicesClass II

ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution.

Veröffentlicht: 21. Januar 2026Rückruf-ID: Z-1093-2026Kategorie: MedizinprodukteLand: Vereinigte Staaten
US
Medical DeviceFDA DevicesUSUS

ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution.

Recalling Firm: Hologic, Inc

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Mitteilung übersetzenTranslate notice text, hazard warnings, and descriptions into any supported language.

Grund für den Rückruf / Gefahr

Fungal contamination of affected lot with Parengyodontium album.

Produktbeschreibung & Identifikation

ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution.

Additional Source Details

FieldValue
CityMarlborough
StateMA
Event id98058
Address 1250 Campus Dr
Code infoCatalog number: 0236004; UDI: (01)25420045508405(17)270303(10)5062EC; UDI-DI: 25420045508405; Lot number: 5062EC.
Postal code01752-3020
Report date20260121
Product typeDevices
Product quantity3,728 units
Reason for recallFungal contamination of affected lot with Parengyodontium album.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20251212
Initial firm notificationLetter
Center classification date20260115

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 ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution.?

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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Übersicht

  • Rückrufendes UnternehmenHologic, Inc
  • StatusOngoing
  • RisikostufeClass II
  • DistributionUS Nationwide distribution.
Recall Hazard Severity
High Alert (Class I)
Offizielle Behördenwarnung

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🚨 SAFETY ALERT: Hologic, Inc - ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution.

Check if your household is affected:
https://therecallfile.com/de/recalls/thinprep-cytolyt-solution-buffered-cell-wash-solution/FDA-Z-1093-2026
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