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139 reported ongoing
140 records in this archive. Latest source date May 7, 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.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Class IReported ongoing
Distribution: US Nationwide distribution including Puerto Rico.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Class IReported ongoing
Distribution: US Nationwide distribution including Puerto Rico.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Class IReported ongoing
Distribution: US Nationwide distribution including Puerto Rico.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Class IReported ongoing
Distribution: US Nationwide distribution including Puerto Rico.
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
Class IIReported ongoing
Distribution: Nationwide and Australia, Canada, S. Korea, Singapore
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
Class IIReported ongoing
Distribution: Nationwide and Australia, Canada, S. Korea, Singapore
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
Class IIReported ongoing
Distribution: Nationwide and Australia, Canada, S. Korea, Singapore
Teleflex LLC is initiating this voluntary field corrective action because the clip cartridges for the affected product is missing a key feature that restricts the application of the clip to the applier. With this step feature missing on the cartridge, the c...
Class IIReported ongoing
Distribution: worldwide
The product contains an expired diluent vial. If the impacted product is used, the sterility of the diluent component cannot be assured as it has passed beyond the studied shelf life of the product.
Class IIReported ongoing
Distribution: US Nationwide
Potential for pilot balloon non-inflation or cuff non-deflation.
Class IIReported ongoing
Distribution: Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, IL, IN, KS, LA, MA, MD, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OH, OK,...
Potential for pilot balloon non-inflation or cuff non-deflation.
Class IIReported ongoing
Distribution: Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, IL, IN, KS, LA, MA, MD, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OH, OK,...
Potential for pilot balloon non-inflation or cuff non-deflation.
Class IIReported ongoing
Distribution: Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, IL, IN, KS, LA, MA, MD, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OH, OK,...
Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.
Class IIReported terminated
Distribution: Domestic distribution to IL, MS, PA, TN.
Product may not be sterile
Class IIReported ongoing
Distribution: TN, CA, NC, TX, FL, OH, MO, IL, OR
Incidents of device splitting or detaching during use
Class IReported ongoing
Distribution: US nationwide distribution
Incidents of device splitting or detaching during use
Class IReported ongoing
Distribution: US nationwide distribution
Incidents of device splitting or detaching during use
Class IReported ongoing
Distribution: US nationwide distribution
Incidents of device splitting or detaching during use
Class IReported ongoing
Distribution: US nationwide distribution
Incidents of device splitting or detaching during use
Class IReported ongoing
Distribution: US nationwide distribution
Incidents of device splitting or detaching during use
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 140 records, including 139 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.