Product Recalls in Louisiana

Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,678 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,678 in last 12 months

Showing 88818900 of 51,202 recalls

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 uncuffed/plain - Murphy Recalled by...

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· Boston Scientific Corporation

Recalled Item: Flexiva Pulse 242 TracTip Single-Use Laser Fibers -intended to be Recalled...

The Issue: Manufactured with the incorrect component may result in lower power output...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

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

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: 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
DrugMay 25, 2023· Golden State Medical Supply Inc.

Recalled Item: Travoprost Ophthalmic Solution Recalled by Golden State Medical Supply Inc....

The Issue: Lack of Assurance of Sterility: Tamper Evidence Seal is missing on secondary...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodMay 25, 2023· ENTRINSIC HEALTH SOLUTION INC

Recalled Item: enterade Advanced Oncology Formula Recalled by ENTRINSIC HEALTH SOLUTION INC...

The Issue: Potential for the product to develop mold and spoil.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMay 24, 2023· T.W. GARNER FOOD CO

Recalled Item: Texas Pete BUFFALO Wing Sauce 12 FL OZ - 355 mL TW GARNER FOOD CO....

The Issue: The product contains undeclared soybean oil and soy lecithin.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 24, 2023· Phadia Ab

Recalled Item: EliA GBM Wells Recalled by Phadia Ab Due to Complaints that specific samples...

The Issue: Complaints that specific samples produced false positive EliA GBM results. A...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2023· Cytocell Ltd.

Recalled Item: RET Distal Probe. Used in Fluorescence in situ hybridization (FISH) Recalled...

The Issue: DNAs used during the manufacture of two affected models were accidentally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2023· NeuMoDx Molecular Inc

Recalled Item: NeuMoDx Cartridge-used for extraction Recalled by NeuMoDx Molecular Inc Due...

The Issue: Top label on some of the NeuMoDx cartridges within these lots may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2023· Cytocell Ltd.

Recalled Item: RET Proximal Probe. Used in Fluorescence in situ hybridization (FISH)...

The Issue: DNAs used during the manufacture of two affected models were accidentally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: Power-PRO 2- A powered ambulance cot that consists of a platform Recalled by...

The Issue: Base leg assembly may bend and result in difficulty engaging/disengaging...

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

Class II — Potential Health HazardOngoing