State
20,322 recalls have nationwide distribution and so reach Mississippi. 0 additional recalls listed Mississippi specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Mississippi consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
TELEFLEX is recalling Slick Set Cuffed Endotracheal Tube and Stylet Sets due to reports that the 15mm connector may disconnect from the tube during use.
TELEFLEX endotracheal tubes are being recalled due to reports of the 15mm connector disconnecting from the tube. The recall affects 860,472 units distributed nationwide, including Puerto Rico.
Teleflex is recalling 47,520 endotracheal tubes due to reported 15mm connector disconnection. The FDA classified this as a Class I recall; disconnected tubes could compromise airway management.
Teleflex LLC recalls 14,780 preformed AGT oral endotracheal tubes due to reports of 15mm connector disconnection. Units were distributed nationwide.
Teleflex LLC is recalling 19,842 preformed oral endotracheal tubes due to reports of 15mm connector disconnection. Affected devices were distributed nationwide.
Teleflex LLC is recalling 1,670 Magill endotracheal tubes (REF 100380055) due to reports of 15mm connector disconnection. The Class I recall affects units distributed nationwide in the US and Puerto Rico.
Teleflex LLC is recalling 7,800 endotracheal tubes due to reports of the 15mm connector disconnecting from the tube. The affected products were distributed nationwide in the US and Puerto Rico.
TELEFLEX LLC is recalling 1,280 endotracheal tubes due to reports of 15mm connector disconnection. The defect could compromise airway management and poses serious safety risks during medical procedures.
Teleflex is recalling 870 units of Slick Set Uncuffed Endotracheal Tubes nationwide due to reports of disconnection of the 15mm connector from the tube.
TELEFLEX is recalling 16,570 units of Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection, which could compromise airway management during use.
Teleflex is recalling approximately 446,163 Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection. The connector failure could affect tube function during patient airway management.
TELEFLEX LLC is recalling Preformed AGT Oral Endotracheal Tubes due to reports of connector disconnection during use, affecting approximately 54,469 units distributed nationwide.
Teleflex endotracheal tubes are recalled nationwide due to reported disconnection of the 15mm connector. The recall affects 1,750 units distributed across the US and Puerto Rico.
TELEFLEX LLC is recalling 3,031 Endotracheal Tube units due to reports of 15mm connector disconnection. The affected Magill model (REF 100380045) was distributed nationwide.
Teleflex is recalling Slick Set endotracheal tubes due to reports of 15mm connector disconnection. The defect could prevent proper airway management during patient care.
Teleflex endotracheal tubes are being recalled due to reports of 15mm connector disconnection. The recall affects approximately 4,110 units distributed nationwide.
TELEFLEX has recalled approximately 50,000 Slick Set Endotracheal Tubes nationwide due to reports of connector disconnection.
Teleflex is recalling 670 units of Preformed AGT Oral Endotracheal Tubes nationwide due to reports of 15mm connector disconnection from the tube.
TELEFLEX is recalling approximately 43,571 units of Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection from the tube, affecting nationwide distribution including Puerto Rico.
TELEFLEX LLC is recalling Slick Set Cuffed Endotracheal Tubes (REF 1700100) due to reports of the 15mm connector disconnecting from the device during use.
TELEFLEX is recalling Preformed AGT Oral Endotracheal Tubes nationwide due to reports of the 15mm connector disconnecting from the tube, affecting 4,155 units.
TELEFLEX endotracheal tubes are being recalled due to potential disconnection of the 15mm connector from the breathing tube. The disconnection could compromise respiratory support in patients.
Teleflex is recalling 31,945 RUSCHELIT Safety Clear Tracheal Tubes nationwide due to reports of 15mm connector disconnection from the endotracheal tube.
Teleflex is recalling approximately 2,550 Slick Set Uncuffed Endotracheal Tubes (REF 150020) due to reports of 15mm connector disconnection.
Teleflex is recalling 8,610 Preformed AGT Oral Endotracheal Tubes nationwide due to reports that the 15mm connector can disconnect from the tube.