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43 reported ongoing
47 records in this archive. Latest source date Jul 26, 2024.
FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
Class IReported ongoing
Distribution: Worldwide
There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
Class IReported ongoing
Distribution: Worldwide
There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
Class IReported ongoing
Distribution: Worldwide
There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
Class IReported ongoing
Distribution: Worldwide
There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
Class IReported ongoing
Distribution: Worldwide
Mislabeling: the corrugate label, lidstock, banner card, and peel sticker accompanying the affected product incorrectly displays a double lumen 5.5 French catheter (and related priming volumes and kit contents for product code ASK-41552-JHVA1), instead of t...
Class IIReported terminated
Distribution: US Nationwide distribution in the state of Florida.
Gravity flow rates on the affected product lidstock are incorrect.
Class IIReported terminated
Distribution: US Nationwide distribution in the states of Florida.
These examples come from this result page and are not a ranking of every recall reason.
This archive contains 47 records, including 43 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.
Compare the product, firm and lot, date, model or serial identifiers with the notice. Use the label-check guide if you need help locating an identifier.
A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.
This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. Check source coverage and the agency's current notices.
Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.