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323 reported ongoing
327 records in this archive. Latest source date Aug 18, 2026.
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.
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Class IIReported ongoing
Distribution: US Nationwide distribution.
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Class IIReported ongoing
Distribution: US Nationwide distribution.
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Class IIReported ongoing
Distribution: US Nationwide distribution.
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Class IIReported ongoing
Distribution: US Nationwide distribution.
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Class IIReported ongoing
Distribution: US Nationwide distribution.
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Class IIReported ongoing
Distribution: US Nationwide distribution.
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Class IIReported ongoing
Distribution: US Nationwide distribution.
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Class IIReported ongoing
Distribution: US Nationwide distribution.
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Class IIReported ongoing
Distribution: US Nationwide distribution.
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Class IIReported ongoing
Distribution: US Nationwide distribution.
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Class IIReported ongoing
Distribution: US Nationwide distribution.
IFU labeling is being updated to revise EtO gas mixture and elimination of reusable cleaning brushes.
Class IIReported ongoing
Distribution: US Nationwide distribution including in the states of AL, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NM, NV, NY, OH, OR, PA, RI, SC, SD, TX,...
The air/water valve MAJ-1444 used with OER-Pro and OER-Elite may become damaged and result in loss of the one-way valve functionality by repeated automated endoscope reprocessing in Olympus OER machines, causing body fluid could backflow into the air/water ...
Class IIReported ongoing
Distribution: US Nationwide distribution.
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Class IReported ongoing
Distribution: US Nationwide Distribution.
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Class IReported ongoing
Distribution: US Nationwide Distribution.
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Class IReported ongoing
Distribution: US Nationwide Distribution.
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Class IReported ongoing
Distribution: US Nationwide Distribution.
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Class IReported ongoing
Distribution: US Nationwide Distribution.
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Class IReported ongoing
Distribution: US Nationwide Distribution.
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Class IReported ongoing
Distribution: US Nationwide Distribution.
These examples come from this result page and are not a ranking of every recall reason.
This archive contains 327 records, including 323 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.