Abbott recalls Infinity 7 implantable pulse generators with serial numbers 05415067030:0023 and 0541:0067020260 due to potential shorter therapy duration than labeled.
Their is a potential that the implantable pulse generator replacement indicator and end of service date may be shorter than indicated in the product labeling potentially resulting in loss of therapy.
Abbott is recalling specific Infinity 7 implantable pulse generators that may stop working earlier than labeled, risking loss of therapy. This affects patients who rely on the device for medical treatment.
The device may indicate a shorter service life than shown on the product label, which could lead to the device stopping therapy before the patient's needs are met. This is a risk for patients who depend on the device for medical treatment.
Patients with Abbott Infinity 7 implantable pulse generators who have the listed serial numbers are affected. Those who require ongoing therapy from the device are most at risk.
Check the serial numbers on your device: 05415067030023 or 05415067020260. These are the only specific models recalled by Abbott Medical.
Look for the serial numbers 05415067030023 or 05415067020260 on your device.
The recall is due to a potential shorter therapy duration than indicated on the product label, which could lead to loss of therapy.
Check your device's serial number to see if it matches the recalled numbers. If it does, contact Abbott Medical for further instructions.
The recall addresses potential therapy loss, not immediate injury risks. The hazard is low risk as it does not involve physical harm.
We’ve drafted a message you can send Abbott Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2431-2024 — Abbott Medical Abbott Medical Hello, I own a Abbott Medical that is covered by recall Z-2431-2024 from Abbott Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
