State
20,307 recalls have nationwide distribution and so reach Tennessee. 0 additional recalls listed Tennessee 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 Tennessee 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 Preformed AGT Oral Endotracheal Tubes due to reports of the 15mm connector disconnecting from the tube. Approximately 2,980 units were distributed nationwide.
TELEFLEX is recalling 5,990 endotracheal tubes due to reports of 15mm connector disconnection. Affected units were distributed nationwide, including Puerto Rico.
TELEFLEX LLC is recalling 300,613 endotracheal tubes due to reports of 15mm connector disconnection. The affected tubes were distributed nationwide and could pose patient safety risks.
Teleflex is recalling 18,353 Flexi-Set Uncuffed Endotracheal Tube sets nationwide due to reports of 15mm connector disconnection. The defect could affect ventilation during use.
Teleflex is recalling endotracheal tubes after reports that the 15mm connector may disconnect from the tube. The recall affects 36,135 units distributed nationwide.
Teleflex recalls preformed AGT oral endotracheal tubes because the 15mm connector may disconnect from the tube, posing risk during patient use.
Teleflex is recalling Slick Set Uncuffed Endotracheal Tube and Stylet Sets due to reports that the 15mm connector may disconnect from the tube. The recall affects 447 units distributed nationwide.
Megadyne Medical Products is recalling 21,100 MEGA SOFT electrosurgery patient return electrodes distributed nationwide due to reports of patient burns during surgical procedures.
Teleflex is recalling Flexi-Set Cuffed Endotracheal Tube Sets due to reported 15mm connector disconnection. The recall affects 92,930 units distributed throughout the United States, including Puerto Rico.
Teleflex is recalling Preformed AGT Oral Endotracheal Tubes due to reports that the 15mm connector may disconnect from the tube. The recall affects 5,120 units distributed nationwide.
Teleflex LLC is recalling approximately 15,810 Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection. The affected units were distributed nationwide, including Puerto Rico.
TELEFLEX is recalling 4,160 endotracheal tubes due to reports of the 15mm connector disconnecting from the tube. Affected units were distributed nationwide.
Teleflex is recalling over 1 million Flexi-Set Cuffed Endotracheal Tube kits due to reports of 15mm connector disconnection from the tube. The recall affects products distributed nationwide.
TELEFLEX LLC is recalling 13,710 units of Flexi-Set Cuffed Endotracheal Tubes due to reports of connector disconnection. The 15mm connector may separate from the tube during use.
Teleflex has recalled 49,050 endotracheal tubes due to reported disconnection of the 15mm connector. Affected units were distributed nationwide, including Puerto Rico.
Teleflex LLC is recalling 19,842 preformed oral endotracheal tubes due to reports of 15mm connector disconnection. Affected devices were distributed nationwide.
TELEFLEX is recalling 5,600 endotracheal tubes nationwide due to reports of 15mm connector disconnection that could compromise airway management during patient care.
Teleflex is recalling Slick Set Uncuffed Endotracheal Tubes due to reported 15mm connector disconnection. The recall affects 22,400 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 is recalling Preformed AGT Oral Endotracheal Tubes due to reports of the 15mm connector disconnecting from the tube. The affected product has been distributed nationwide.
Teleflex is recalling Slick Set Cuffed Endotracheal Tube and Stylet Sets due to reports of disconnection of the 15mm connector from the endotracheal tube. The affected units were distributed nationwide.
Teleflex is recalling Slick Set Cuffed Endotracheal Tubes nationwide due to reported disconnection of the 15mm connector from the tube, affecting airway management in critical care settings.
Teleflex is recalling 19,250 endotracheal tubes because the 15mm connector may disconnect during use, potentially compromising airway management in patients.
Teleflex is recalling 37,890 Preformed AGT endotracheal tubes due to reports of 15mm connector disconnection. The devices were distributed nationwide in the United States and Puerto Rico.
Teleflex recalls 53,216 Preformed AGT Endotracheal Tubes due to reported disconnection of the 15mm connector. Affected units were distributed nationwide including Puerto Rico.