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T34 Syringe Pump

Veröffentlicht: 10. März 2021Rückruf-ID: 6cb90fcd-6180-4a37-9877-be481a8ba7deKategorie: VerbraucherprodukteLand: Australien
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Mitteilung übersetzenTranslate notice text, hazard warnings, and descriptions into any supported language.

Grund für den Rückruf / Gefahr

The voltage of the 9V/6LR61 battery may drop prematurely or earlier than expected in T34 2nd and 3rd edition devices. This may cause an interruption to the infusion, following events of: 1. Premature 'low battery' or 'end battery' alarms 2. Unexpected pump shut down with or without alarm. Battery brands/lots that have lower and more stable internal resistance are not likely to cause significant voltage dips and therefore not likely to trigger early low/end battery alarms or pump shut down.

Produktbeschreibung & Identifikation

Reason / Defects: The voltage of the 9V/6LR61 battery may drop prematurely or earlier than expected in T34 2nd and 3rd edition devices. This may cause an interruption to the infusion, following events of: 1. Premature 'low battery' or 'end battery' alarms 2. Unexpected pump shut down with or without alarm. Battery brands/lots that have lower and more stable internal resistance are not likely to cause significant voltage dips and therefore not likely to trigger early low/end battery alarms or pump shut down. Hazards: If there is an interruption to the infusion, or the pump shuts down unexpectedly, this could result in the patient receiving insufficient delivery of medication or fluids, which can lead to serious health complications. What to do: REM Systems will contact affected customers in writing. Consumers are requested to take the following actions for devices currently in clinical use: 1. Continue use of the device with 9V/6LR61 type batteries as per the Directions For Use (DFU) instructions; 2. As a precaution, always have a spare set of high quality batteries; 3. Be mindful that battery life may be affected by factors such as temperature and battery manufacturer; 4. Maintain infusion monitoring and best clinical practices to detect and react to system alarms as per DFU instructions; and 5. Report without delay any device complaint including events of early/premature battery alarms, or any instances of unexpected pump shut down without alarm. For further information, contact REM Systems Customer Service by phone on 1800 737 222

Betroffene Produkte

T34 Syringe Pump All serial numbers ARTG 131232 (REM Systems Pty Ltd - Infusion pump, syringe) For the provision of small dose infusion therapy, the T34 Syringe Pump gradually administers small precise amounts of fluid and/or medications to a patient.

Additional Source Details

FieldValue
Guid › #text6cb90fcd-6180-4a37-9877-be481a8ba7de
Guid › @ is Perma Linkfalse
Linkhttps://www.productsafety.gov.au/search-consumer-product-recalls/t34-syringe-pump
Pub DateWed, 10 Mar 2021 00:00:00 +0000
Extracted imagehttps://www.productsafety.gov.au/system/files/styles/large/private/T34%20Syringe%20Pump.jpg?itok=aGKI5-O1

Consumer Action Protocol: What You Should Do Immediately

Safety Steps
1Verify Product Identifiers

Check the model number, serial number, and date stamp on the rating label on the back or underside of the product.

2Isolate & Discontinue Use

Immediately discontinue using the product. Unplug electrical items and keep juvenile items out of reach of children.

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 (Australia Products).

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 T34 Syringe Pump?

Immediately stop using the product and keep it out of reach of children. Disconnect power if electrical, and do not attempt makeshift home repairs.

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 (Australia Products). 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

  • RisikostufePharmacy and medical products
  • DistributionAustralia
Recall Hazard Severity
Caution (Class III)
Offizielle Behördenwarnung

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