ZOLL Circulation, Inc. - Product Catalog
ZOLL Circulation, Inc. offers a range of medical devices and products for circulation monitoring and patient care.
Lower-risk recall
Due to increase in Li-Ion Battery failures
Contact the company
What happened, in plain English
ZOLL Circulation, Inc. is a medical device company specializing in circulation monitoring and patient care solutions. Their products include various medical devices for monitoring and managing patient circulation. Read more at govinfonow.com/recall/60030-zoll-circulation-inc-product-catalog.
Source Summary by GovInfoNow · govinfonow.com/recall/60030-zoll-circulation-inc-product-catalog · Updated September 23, 2026 · FDA enforcement record: FDA #Z-0118-2023
Cite this page
“ZOLL Circulation, Inc. - Product Catalog.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/60030-zoll-circulation-inc-product-catalog. Based on FDA recall #Z-0118-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0118-2023%22&limit=1).
Why it’s dangerous
Low risk of harm as the products are designed for medical use and follow safety standards.
Who’s affected
Patients, healthcare professionals, medical facilities
How to tell if you have this one
Check for proper medical certification, compliance with regulatory standards (e.g., FDA), and manufacturer recommendations.
- Brand
ZOLL Circulation, Inc.- Category
Medical device
What to do — step by step
What to do if you find a product with this brand
Ensure the product is certified by the relevant regulatory body (e.g., FDA in the US).
How to verify the product's safety
Check for the product's regulatory certification and compliance with medical standards.
Where it went and when
Where it was distributed
Distributed in 46 states and Puerto Rico, and outside the U.S.
FDA distribution: “U.S.: AK, AL, AR, AZ, CA, CO, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, Puerto Rico, RI, SC, RN, TX, UT, VA, VT, Virgin Islands, WA, WI, WV and WY. O.U.S.:…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, 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, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming.
Recall timeline
FDA published this recall 41 days 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.
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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-0118-2023 (September 22, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0118-2023 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 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.