Product Recalls in Connecticut

Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,636 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,636 in last 12 months

Showing 60816100 of 28,245 recalls

Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Murphy Recalled by TELEFLEX...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal Murphy Eye Recalled by TELEFLEX LLC Due to...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal Magill Recalled by TELEFLEX LLC Due to Reports...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: RUSCHELIT Safety Clear Tracheal Tube Recalled by TELEFLEX LLC Due to Reports...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal Murphy Eye Recalled by TELEFLEX LLC Due to...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Flexi-Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal Magill Recalled by TELEFLEX LLC Due to Reports...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Murphy Recalled by TELEFLEX...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Flexi-Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal Magill Recalled by TELEFLEX LLC Due to Reports...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing