Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

3051–3075 of 6105

SevereFDA (Food)·F-1299-2023·2023-07-05
Sun Wave Brand Jelly Cup Recalled for Potential Choking Hazard
Richin Trading Inc is recalling 141,192 units of Sun Wave Brand Jelly Cup due to a potential choking hazard. Affected products were distributed across 17 US states.
Product
Sun Wave Brand Jelly Cup (Assorted Flavors); Made in Taiwan; Item Number 12151; UPC 715685121512; Net Weight 35.27 oz. (1000 g) Sun Wave Brand Jelly Cup (Assorted Flavors); Made in Taiwan; Item Number 12143; UPC 715685121437; Net Weight 52.91 oz. (1500 g)
Category
Food
Distribution
17 states
SevereFDA (Devices)·Z-1933-2023·2023-07-05
Teleflex Endotracheal Tubes Recalled for 15mm Connector Disconnection
Teleflex is recalling 190 endotracheal tubes due to reports of the 15mm connector disconnecting from the tube. This disconnection could compromise airway management and ventilation.
Product
Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380065
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1847-2023·2023-07-05
Flexi-Set Endotracheal Tubes recalled for connector disconnection risk
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.
Product
Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504560
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1839-2023·2023-07-05
Endotracheal Tube Connector Disconnection Risk Prompts Teleflex Recall
Teleflex is recalling Slick Set Uncuffed Endotracheal Tubes due to reported 15mm connector disconnection. The recall affects 22,400 units distributed nationwide.
Product
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170130
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1885-2023·2023-07-05
Teleflex endotracheal tubes recalled due to connector disconnection
Teleflex has recalled 49,050 endotracheal tubes due to reported disconnection of the 15mm connector. Affected units were distributed nationwide, including Puerto Rico.
Product
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082055
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1961-2023·2023-07-05
TELEFLEX Endotracheal Tubes Recalled for Connector Disconnection Risk
TELEFLEX is recalling 17,950 endotracheal tubes due to reports of the 15mm connector disconnecting from the device. These are critical airway support devices.
Product
Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080070
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1861-2023·2023-07-05
Preformed Endotracheal Tube Connector Disconnection Recall by TELEFLEX
TELEFLEX LLC is recalling 3,100 preformed oral endotracheal tubes nationwide due to reports of 15mm connector disconnection that could compromise airway management.
Product
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180030
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1951-2023·2023-07-05
Endotracheal Tube Connector Disconnection Recalled by Teleflex
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.
Product
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781035
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1838-2023·2023-07-05
Teleflex Slick Set Endotracheal Tube Connector Disconnection Recall
Teleflex is recalling 18,900 Slick Set Uncuffed Endotracheal Tubes due to reports of 15mm connector disconnection. The affected units were distributed nationwide in the United States and Puerto Rico.
Product
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170125
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1941-2023·2023-07-05
Endotracheal Tube Connector Disconnection Recall Due to Device Malfunction
Teleflex is recalling 20,042 endotracheal tubes due to reports of 15mm connector disconnection that could compromise airway management. The FDA classified this as a Class I recall.
Product
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780040
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1853-2023·2023-07-05
Flexi-Set Cuffed Endotracheal Tube and Stylet Connector Disconnection Recall
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.
Product
Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504590
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1955-2023·2023-07-05
Preformed AGT Endotracheal Tubes Recalled for Connector Disconnection
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.
Product
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781065
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1934-2023·2023-07-05
Endotracheal Tubes With 15mm Connector Disconnection Recalled Nationwide
TELEFLEX is recalling 25,630 endotracheal tubes nationwide because the 15mm connector can disconnect. The affected products were distributed throughout the United States and Puerto Rico.
Product
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382025
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1849-2023·2023-07-05
Flexi-Set Endotracheal Tubes recalled for connector disconnection
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.
Product
Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504570
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1884-2023·2023-07-05
Teleflex Endotracheal Tubes Recalled Due to Connector Disconnection
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.
Product
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082050
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1894-2023·2023-07-05
Endotracheal tubes recalled for 15mm connector disconnection
Teleflex is recalling 19,250 endotracheal tubes because the 15mm connector may disconnect during use, potentially compromising airway management in patients.
Product
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082100
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1877-2023·2023-07-05
Endotracheal Tube Connector Disconnection Risk, FDA Class I Recall
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.
Product
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780075
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1872-2023·2023-07-05
Preformed AGT Endotracheal Tubes Recalled Nationwide for Connector Disconnection
Teleflex recalls 53,216 Preformed AGT Endotracheal Tubes due to reported disconnection of the 15mm connector. Affected units were distributed nationwide including Puerto Rico.
Product
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181045
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1870-2023·2023-07-05
Preformed AGT Oral Endotracheal Tubes recalled for connector disconnection risk
TELEFLEX is recalling 2,874 Preformed AGT Oral Endotracheal Tubes nationwide due to reports of the 15mm connector disconnecting from the tube. Affected users should immediately discontinue use.
Product
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181030
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1862-2023·2023-07-05
Preformed AGT Endotracheal Tubes Recalled for Connector Disconnection Risk
Teleflex is recalling 4,769 endotracheal tubes due to reports of 15mm connector disconnection. This defect could interrupt breathing support during airway management procedures.
Product
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180035
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1939-2023·2023-07-05
Endotracheal Tubes Recalled for Connector Disconnection by Teleflex
TELEFLEX LLC is recalling 2,140 endotracheal tubes nationwide due to reports of the 15mm connector disconnecting from the tube. Affected units were distributed throughout the United States, including Puerto Rico.
Product
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382065
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1901-2023·2023-07-05
Slick Set Endotracheal Tubes recalled for connector disconnection
TELEFLEX is recalling 2,382 Slick Set Uncuffed Endotracheal Tubes due to reports of 15mm connector disconnection. Units were distributed nationwide including Puerto Rico.
Product
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150025
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1953-2023·2023-07-05
Endotracheal Tubes Recalled for Potential 15mm Connector Disconnection
TELEFLEX LLC is recalling Preformed AGT Oral Endotracheal Tubes because the 15mm connector may disconnect from the tube, creating a potential airway access risk.
Product
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781055
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1959-2023·2023-07-05
Endotracheal Tubes Recalled for Potential 15mm Connector Disconnection
TELEFLEX is recalling 4,160 endotracheal tubes due to reports of the 15mm connector disconnecting from the tube. Affected units were distributed nationwide.
Product
Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080060
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1880-2023·2023-07-05
Endotracheal Tubes Recalled Due to Connector Disconnection Risk
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.
Product
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781075
Category
Medical Device
Distribution
Distributed nationwide

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