State
20,324 recalls have nationwide distribution and so reach Delaware. 0 additional recalls listed Delaware 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 Delaware 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 LLC is recalling Flexi-Set Cuffed Endotracheal Tube and Stylet Sets nationwide due to reports of connector disconnection. The affected devices may disconnect during use, potentially compromising airway management.
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 is recalling Slick Set Uncuffed Endotracheal Tubes due to reported 15mm connector disconnection. The recall affects 22,400 units distributed nationwide.
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 endotracheal tubes after reports that the 15mm connector may disconnect from the tube. The recall affects 36,135 units distributed nationwide.
Teleflex recalls 76,060 preformed oral endotracheal tubes due to reports of 15mm connector disconnection. A disconnected connector could compromise ventilation in critical care settings.
Teleflex LLC is recalling 17,840 Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection. These tubes have been distributed nationwide including Puerto Rico.
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 LLC is recalling 690 endotracheal tubes with high-volume, low-pressure cuff due to reports of connector disconnection. The affected products were distributed nationwide.
Teleflex is recalling Slick Set Uncuffed Endotracheal Tubes due to reports of the 15mm connector disconnecting from the tube. The recall affects 14,160 units distributed nationwide.
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 31,945 RUSCHELIT Safety Clear Tracheal Tubes nationwide due to reports of 15mm connector disconnection from the endotracheal tube.
Teleflex LLC is recalling 670 endotracheal tubes due to reports that the 15mm connector is disconnecting from the tube. Affected units were distributed nationwide including Puerto Rico.
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 Slick Set Uncuffed Endotracheal Tubes due to reports of disconnection of the 15mm connector. The affected products have been distributed nationwide including Puerto Rico.
Teleflex recalls preformed AGT oral endotracheal tubes because the 15mm connector may disconnect from the tube, posing risk during patient use.
Hyundai is recalling certain 2020-2022 Accent and 2021-2022 Elantra models due to seat belt pretensioners that may explode during a crash, potentially projecting metal fragments and injuring occupants. Dealers will secure them with a cap at no charge.
TELEFLEX LLC is recalling Flexi-Set Cuffed Endotracheal Tube and Stylet Sets nationwide due to reports of the 15mm connector disconnecting from the tube, posing a serious risk in critical care settings.
Teleflex is recalling 1,110 endotracheal tubes due to reports of 15mm connector disconnection. The affected units are distributed nationwide in the US and Puerto Rico.
Teleflex is recalling 12,400 Flexi-Set Uncuffed Endotracheal Tube and Stylet Sets nationwide due to reports of 15mm connector disconnection. The affected batches and lot numbers are identified above.
Teleflex is recalling 17,551 units of Flexi-Set Uncuffed Endotracheal Tubes nationwide after reports of the 15mm connector disconnecting from the tube.
TELEFLEX is recalling 5,600 endotracheal tubes nationwide due to reports of 15mm connector disconnection that could compromise airway management during patient care.
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 670 units of Preformed AGT Oral Endotracheal Tubes nationwide due to reports of 15mm connector disconnection from the tube.
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.