Abbott Medical - Medical Devices and Equipment
Abbott Medical provides a wide range of medical devices and equipment for healthcare professionals. Our products are designed to improve patient outcomes and enhance clinical efficiency.
Lower-risk recall
Their is a potential that electromagnetic interference may cause leadless pacemaker may result in mode change.
Contact the company
What happened, in plain English
Abbott Medical is a leading manufacturer of medical devices and equipment. They offer products that help healthcare professionals improve patient outcomes and enhance clinical efficiency. Their products are used in various healthcare settings including hospitals, clinics, and laboratories. Read more at govinfonow.com/recall/56203-abbott-medical-medical-devices-and-equipment.
Source Summary by GovInfoNow · govinfonow.com/recall/56203-abbott-medical-medical-devices-and-equipment · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1695-2024
Cite this page
“Abbott Medical - Medical Devices and Equipment.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/56203-abbott-medical-medical-devices-and-equipment. Based on FDA recall #Z-1695-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1695-2024%22&limit=1).
Why it’s dangerous
Low risk of harm due to the nature of medical devices and equipment. Products are designed to be safe and effective for clinical use.
Who’s affected
Healthcare professionals, patients
How to tell if you have this one
Check for proper certification and compliance with medical standards such as FDA, CE marking, and ISO standards.
- Brand
Abbott Medical- Category
Medical device
What to do — step by step
What to do if you find a product
If you find a product that is not certified or does not meet medical standards, contact Abbott Medical directly or report it to the relevant regulatory authority.
How to verify product authenticity
Verify the product by checking for official certification marks, such as FDA approval, CE marking, or ISO certification. Ensure the product comes from an authorized distributor.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 48 states.
FDA distribution: “US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin.
Recall timeline
FDA published this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
How can I ensure the safety of Abbott Medical products?
Abbott Medical products undergo rigorous testing and quality control processes to ensure safety and efficacy. They are certified by regulatory bodies such as the FDA and CE marking.
Where can I find more information about Abbott Medical products?
Visit the Abbott Medical website or contact their customer support for detailed product information and specifications.
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Where this comes from
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.
- Official source: FDA Recall #Z-1695-2024 (February 5, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1695-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.