State
20,307 recalls have nationwide distribution and so reach Maryland. 0 additional recalls listed Maryland 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 Maryland 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 of disconnection of the 15mm connector from the endotracheal tube. The affected units were distributed nationwide.
TELEFLEX has recalled approximately 50,000 Slick Set Endotracheal Tubes nationwide due to reports of connector disconnection.
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 LLC is recalling 6,710 endotracheal tubes due to reports of 15mm connector disconnection. This Class I recall affects units distributed nationwide.
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 is recalling approximately 2,550 Slick Set Uncuffed Endotracheal Tubes (REF 150020) due to reports of 15mm connector disconnection.
Megadyne Medical Products is recalling MEGA SOFT Universal Patient Return Electrodes after reports of patient burns during electrosurgery procedures. The FDA classified this as a Class I recall.
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 8,610 Preformed AGT Oral Endotracheal Tubes nationwide due to reports that the 15mm connector can disconnect from the tube.
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 Slick Set endotracheal tubes due to reports of 15mm connector disconnection. The defect could prevent proper airway management during patient care.
Teleflex LLC is recalling 17,102 Endotracheal Tubes (REF 100382040) following reports of disconnection of the 15mm connector from the tube. The affected units were distributed nationwide, including Puerto Rico.
Megadyne Medical Products recalls approximately 21,100 MEGADYNE MEGA SOFT Pediatric Patient Return Electrodes (Model 0840) due to reports of patient burns during electrosurgical procedures.
TELEFLEX is recalling 1,570 units of Preformed AGT Oral Endotracheal Tubes nationwide due to reports of 15mm connector disconnection from the tubes. The disconnection could compromise airway management during patient ventilation.
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.
Megadyne Medical Products is recalling 21,100 MEGADYNE MEGA SOFT Reusable Patient Return Electrodes nationwide due to reports of patient burns during electrosurgical procedures.
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 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 3,309 Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection. This defect may compromise airway management during medical 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 recalls 53,216 Preformed AGT Endotracheal Tubes due to reported disconnection of the 15mm connector. Affected units were 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 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 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 is recalling Slick Set Cuffed Endotracheal Tubes due to reports of the 15mm connector disconnecting from the tube, which could interrupt airway support during mechanical ventilation.