Abbott recalls Infinity 5 implantable pulse generators with potential for shorter therapy duration than labeled. Affected units have specific serial numbers. Contact Abbott for replacement.
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 certain Infinity 5 implantable pulse generators that may stop working earlier than labeled, risking loss of therapy. This affects patients with specific serial numbers.
The replacement indicator and end of service date on the device may be shorter than shown on the product label. This could lead to the device stopping therapy before the intended time, potentially causing loss of medical treatment.
Patients with the recalled Infinity 5 pulse generators who have specific serial numbers. Those at highest risk are individuals relying on the device for medical therapy.
Check if your device has serial numbers 05415067030016 or 05415067020246. These units were sold with the specific reference number REF: 6660 and SterileEO.
Look for the serial numbers 05415067030016 or 05415067020246 on your device.
The recall is because the replacement indicator and end of service date may be shorter than indicated on the product label, potentially causing loss of therapy.
Check your device's serial number. If it matches 05415067030016 or 05415067020246, contact Abbott Medical for replacement.
The recall addresses potential loss of therapy, not immediate injury risks. The hazard level 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-2429-2024 — Abbott Medical Abbott Medical Hello, I own a Abbott Medical that is covered by recall Z-2429-2024 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.
