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LIFEPAK CR2 Defibrillator

Veröffentlicht: 22. April 2021Rückruf-ID: 9f9cd737-0210-4a7d-9cfb-cac12e7348fbKategorie: VerbraucherprodukteLand: Australien
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Mitteilung übersetzenTranslate notice text, hazard warnings, and descriptions into any supported language.

Grund für den Rückruf / Gefahr

The LIFEPAK CR2's lid magnet may dislodge from the device. The lid magnet is the primary means by which the device will turn on and off when the lid is opened or closed. If the battery dislodges: 1. The battery may be depleted prematurely, even if the device is not powered on; and 2. Users may not be able to turn the device on if they do not use the on/off button or if the battery has fully depleted.

Produktbeschreibung & Identifikation

Reason / Defects: The LIFEPAK CR2's lid magnet may dislodge from the device. The lid magnet is the primary means by which the device will turn on and off when the lid is opened or closed. If the battery dislodges: 1. The battery may be depleted prematurely, even if the device is not powered on; and 2. Users may not be able to turn the device on if they do not use the on/off button or if the battery has fully depleted. Hazards: If the battery has been depleted or users do not turn the device on, the device will not work and will not be available to defibrillate a patient in an emergency. What to do: Stryker is contacting all customers to provide Supplemental Instructions and replacement accessories, where needed. Affected consumers are advised to perform the following for all LIFEPAK CR2 Defibrillators: 1. Inspect the defibrillator and record the item and serial number of the device on the customer response form. 2. Review and retain the Supplemental Instructions attached to the customer letter. 3. Inspect the lid for the presence of a magnet as per the instructions in the customer letter. 4. Conduct a Device Readiness check in accordance with the LIFEPAK CR2 Operating Instructions, maintaining a State of Readiness (pp. 77-78), and the Supplemental Instructions provided with the customer letter. 5. Return the customer response form to Stryker or a distributor, indicating the results of these inspections and checks. If consumers have a device which does not turn on when the lid is opened, they can continue to use it by using its power button to turn it on and off and follow the updated operating instructions. For further information, consumers can contact the Stryker Post Market Team on postmarketssp@stryker.com or 0427 540 168.

Betroffene Produkte

LIFEPAK CR2 defibrillators are automated external defibrillators (AEDs) used in cases of life-threatening irregular heartbeat that leads to Sudden Cardiac Arrest (SCA) ARTG 282772 (Stryker Australia Pty Ltd - Non-rechargeable public automated external defibrillator)

Additional Source Details

FieldValue
Guid › #text9f9cd737-0210-4a7d-9cfb-cac12e7348fb
Guid › @ is Perma Linkfalse
Linkhttps://www.productsafety.gov.au/search-consumer-product-recalls/lifepak-cr2-defibrillator
Pub DateThu, 22 Apr 2021 00:00:00 +0000
Extracted imagehttps://www.productsafety.gov.au/system/files/styles/large/private/LIFEPACK%20CR2%20Defibrillator.png?itok=NnyV6Xsx

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 LIFEPAK CR2 Defibrillator?

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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🚨 SAFETY ALERT: LIFEPAK CR2 Defibrillator

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https://therecallfile.com/de/recalls/lifepak-cr2-defibrillator/AU-9f9cd737-0210-4a7d-9cfb-cac12e7348fb
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