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 81618180 of 51,202 recalls

FoodAugust 11, 2023· Great Lakes Cheese, Inc.

Recalled Item: Pasteurized Prepared Cheese Product Recalled by Great Lakes Cheese, Inc. Due...

The Issue: pasteurized process cheese products may not be at customer level due to...

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

Class III — Low RiskOngoing
Refund
FoodAugust 11, 2023· Great Lakes Cheese, Inc.

Recalled Item: Harris Tetter Cheesy Melt Recalled by Great Lakes Cheese, Inc. Due to...

The Issue: pasteurized process cheese products may not be at customer level due to...

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

Class III — Low RiskOngoing
Refund
FoodAugust 11, 2023· Lyons Magnus LLC

Recalled Item: Lyons Grape Juice packaged in 4 fl oz opaque white plastic cup 96 cups per...

The Issue: Signs of bloating in juice cups

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 11, 2023· Lyons Magnus LLC

Recalled Item: GFS Harvest Valley Cranberry/Grape Juice packaged in 4 fl oz Recalled by...

The Issue: Signs of bloating in juice cups

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 11, 2023· Lyons Magnus LLC

Recalled Item: GFS Harvest Valley Grape Juice packaged in 4 fl oz Recalled by Lyons Magnus...

The Issue: Signs of bloating in juice cups

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2023· Imprimis NJOF, LLC

Recalled Item: Moxifloxacin - Bromfenac Sterile Ophthalmic Solution 0.5% / 0.075% Recalled...

The Issue: Subpotent Drug; sub-potent Bromfenac levels, below the 90.0-110.0%...

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

Class III — Low RiskOngoing
Refund
DrugAugust 10, 2023· Colgate Palmolive Company

Recalled Item: hello wild strawberry fluoride toothpaste Recalled by Colgate Palmolive...

The Issue: Labeling: Label Mix-Up: Some hello wild strawberry fluoride toothpaste,...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 10, 2023· Conopco DBA Unilever

Recalled Item: Knorr Fideos con Tomate Tomato Based Pasta Soup Mix 3.5 oz Recalled by...

The Issue: Undeclared egg

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 10, 2023· Conopco DBA Unilever

Recalled Item: Knorr Letras con Tomate Tomato Based Alphabet Pasta Soup Mix Recalled by...

The Issue: Undeclared egg

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 10, 2023· Conopco DBA Unilever

Recalled Item: Knorr Estrellitas con Tomate Tomato Based Star Pasta Soup Mix Recalled by...

The Issue: Undeclared egg

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 10, 2023· Nestle-USA, Inc. (Corporate Office)

Recalled Item: Nestle Toll House Recalled by Nestle-USA, Inc. (Corporate Office) Due to...

The Issue: Potential presence of wood fragments.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 10, 2023· Turncare, Inc

Recalled Item: Brand Name: Guardian 2 System Product Name: Guardian System 2 Recalled by...

The Issue: A software update corrected an issue where "low" and "terminal" battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Covidien

Recalled Item: McGrath Mac 2 Recalled by Covidien Due to Laryngoscope blades may contain an...

The Issue: Laryngoscope blades may contain an ineffective application of anti-fog agent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Covidien

Recalled Item: McGrath Mac 2 Recalled by Covidien Due to Laryngoscope blades may contain an...

The Issue: Laryngoscope blades may contain an ineffective application of anti-fog agent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran : Endobronchial Always on Track Models: INS-0392 AOTT 21ga Needle...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran : Percutaneous Always on Track Models: INS-5040 Always-On vTrack...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran:SPiN Thoracic Navigation System Models: SYS-4230 SPiN Thoracic...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran : Percutaneous Models: INS-5620 SPiN Perc Biopsy Needle Guide Kit -...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran : Endobronchial Models: INS-5500 View Optical Probe INS-5450 SPiN...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran Endobronchial: Models: INS-5925 SPiN Access Catheter¿ 180 Degree for...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing