FDA recall record

Abbott Infinity 7, Implantable Pulse Generator, REF: 6663, SterileEO, Rx Only recall — FDA Z-2432-2024

Their is a potential that the implantable pulse generator replacement indicator and end of service date may be shorter than indicated in the product…

Class IIclassification
Z-2432-2024official record ID
Jul 31, 2024report date

Recall record at a glance

Official recordZ-2432-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmAbbott Medical
Report dateJul 31, 2024
Recall initiation dateMay 22, 2024
Quantity1198 units
LocationPlano, TX, United States

Official product description

Abbott Infinity 7, Implantable Pulse Generator, REF: 6663, SterileEO, Rx Only

Why the product was recalled

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.

Distribution information

Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, DC, FL, GA, IL, IN, KY, LA, MA, MD, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NY, OH, OK, OR, PA, PR, SC, TX, UT, VA, WA, WI, WY and the countries of Algeria, Argentina, Australia, Austria, Belgium, Brazil, Canada, Colombia, Cyprus, Czech Republic, Ecuador, Estonia, Finland, France, Germany, Greece, Hungary, India, Ireland, Israel, Italy, Japan, Jordan, Korea, Lithuania, Mexico, Netherlands, Norway, Pakistan, Poland, Portugal, Russian Federation, Saudi Arabia, South Africa, Spain, Sweden, Taiwan, Turkey, United Arab Emirates, United Kingdom.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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