Accueil/Tous les Rappels/FDA-Z-3011-2026
FDA DevicesClass II

Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

Publié le: 2 septembre 2026ID du rappel: Z-3011-2026Catégorie: Dispositifs MédicauxPays: États-Unis
US
Medical DeviceFDA DevicesUSUS

Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

Recalling Firm: AVID Medical, Inc.

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

Motif du rappel / Danger

Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

Description du produit & Identification

Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

Produits concernés

Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

Additional Source Details

FieldValue
CityToano
StateVA
Event id99527
Address 19000 Westmont Dr
Address 2N/A
Code infoLot Code: Lot Number: 1649519 UDI: 10809160457887
Postal code23168-9351
Report date20260902
Product typeDevices
Product quantity78 kits
Reason for recallLabeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260709
Initial firm notificationLetter
Center classification date20260821

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 Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03?

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 responsableAVID Medical, Inc.
  • StatusOngoing
  • Niveau de risqueClass II
  • DistributionUS Nationwide distribution in the states of MS, TX.
Recall Hazard Severity
High Alert (Class I)
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🚨 SAFETY ALERT: AVID Medical, Inc. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

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https://therecallfile.com/fr/recalls/halyard-total-joint-model-catalog-number-msbm036-03/FDA-Z-3011-2026
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