FDA DevicesClass II

Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;

Publicado: 18 de marzo de 2026ID de Retiro: Z-1513-2026Categoría: Dispositivos MédicosPaís: Estados Unidos
US
Medical DeviceFDA DevicesUSUS

Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;

Recalling Firm: Waldemar Link GmbH & Co. KG (Mfg Site)

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Motivo del Retiro / Peligro

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

Descripción del Producto e Identificación

Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;

Productos Afectados

Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;

Additional Source Details

FieldValue
CityNorderstedt
StateN/A
Event id98342
Address 1Ost Str. 4-10
Address 2N/A
Code infoItem Number: 16-2840/02; UDI-DI: 04026575359233; Serial/Lot Number: 250925/0640 , 250925/0641, 250925/0642, 250925/0646, 250925/0650, 250925/0652, 250925/0653 , 250925/0656, 250925/0658, 250925/0669, 250925/0670, 250925/0680, 250925/0681 , 250925/0682, 250925/0687, 250925/0689, 250925/0690, 250925/0691, 250925/0693 , 250925/0694, 251110/3293, 250925/0660, 250925/0661, 250925/0684, 250925/0685 , 250925/0657, 250925/0663, 250925/0659, 250925/0678, 251110/3288, 251110/3292 , 251110/3303, 251110/3313, 250925/0683, 250925/0674, 250925/0644, 250925/0665 , 250925/0668, 250925/0671, 250925/0673, 250925/0676, 250925/0664 , 250925/0651 , 251110/3297, 251110/3289, 250925/0639, 250925/0648, 250925/0688, 250925/0696;
Postal codeN/A
Report date20260318
Product typeDevices
Product quantity49 units (OUS only)
Reason for recallThe potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260112
Initial firm notificationLetter
Center classification date20260310

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 Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;?

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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Resumen

  • Empresa ResponsableWaldemar Link GmbH & Co. KG (Mfg Site)
  • StatusOngoing
  • Nivel de RiesgoClass II
  • DistributionWorldwide - US Nationwide distribution in the state of NJ and the countries of Belarus, Canada, Switzerland , Colombia, Germany, Spain, United Kingdom, Hungary, India, Italy, Netherlands, Romania, Saudi Arabia.
Recall Hazard Severity
High Alert (Class I)
Alerta Oficial de la Agencia

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🚨 SAFETY ALERT: Waldemar Link GmbH & Co. KG (Mfg Site) - Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;

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https://therecallfile.com/es/recalls/endo-model-sl-connection-component-incl-pe-plateau-item-number-16-2840/FDA-Z-1513-2026
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