Accueil/Tous les Rappels/FDA-Z-1816-2026
FDA DevicesClass II

Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

Publié le: 22 avril 2026ID du rappel: Z-1816-2026Catégorie: Dispositifs MédicauxPays: États-Unis
US
Medical DeviceFDA DevicesUSUS

Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

Recalling Firm: Integra LifeSciences Corp. (NeuroSciences)

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Motif du rappel / Danger

Increased rate of out-of-specification endotoxin results.

Description du produit & Identification

Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

Additional Source Details

FieldValue
CityPrinceton
StateNJ
Event id98607
Address 11100 Campus Rd
Address 2N/A
Code infoProduct ID: WSM0505. UDI-DI: 00386190001431. Lot Numbers: 7579683, 7583933, 7583891, 7583935, 7594266, 7594286, 7593011.
Postal code08540-6650
Report date20260422
Product typeDevices
Product quantity148 units
Reason for recallIncreased rate of out-of-specification endotoxin results.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260319
Initial firm notificationLetter
Center classification date20260415

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 Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.?

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 responsableIntegra LifeSciences Corp. (NeuroSciences)
  • StatusOngoing
  • Niveau de risqueClass II
  • DistributionUS Nationwide distribution in the states of AL, AZ, CA, DC, FL, GA, IA, IL, KS, KY, LA, MD, ME, MN, MO, MT, NC, ND, NE, NJ, NY, OH, PA, SC, SD, TN, TX, VA, VT, WA, WI, WV.
Recall Hazard Severity
High Alert (Class I)
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🚨 SAFETY ALERT: Integra LifeSciences Corp. (NeuroSciences) - Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

Check if your household is affected:
https://therecallfile.com/fr/recalls/cytal-wound-matrix-2-layer-5x5-cm-product-id-wsm0505/FDA-Z-1816-2026
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