Abbott Medical 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 Medical is recalling certain Infinity 5 implantable pulse generators that may stop working earlier than labeled, risking loss of therapy. This affects patients who need consistent medical treatment from the device.
The replacement indicator and end-of-service date on the device may be shorter than what's shown on the product label. This could mean the device stops working before the intended therapy period ends, leading to loss of medical treatment.
Patients with Abbott Infinity 5 implantable pulse generators who have the specific serial numbers listed. Those at highest risk are individuals relying on the device for life-sustaining therapy.
Check your device's serial number against the list: 05415067020253. This is the only identifier provided for affected units.
Look for the serial number on your Abbott Infinity 5 pulse generator. If it matches 05415067020253, it's affected.
The recall is because the replacement indicator and end-of-service date may be shorter than labeled, potentially causing loss of therapy.
Check your device's serial number. If it matches 05415067020253, contact Abbott Medical for a replacement.
The recall is about potential loss of therapy, not direct injury risk. The hazard does not involve physical harm like falls or fires.
We’ve drafted a message you can send Abbott Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2430-2024 — Abbott Medical Abbott Medical Hello, I own a Abbott Medical that is covered by recall Z-2430-2024 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.
