Product Recalls in Tennessee

Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,110 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,110 in last 12 months

Showing 8361–8380 of 52,000 recalls

FoodAugust 11, 2023· Great Lakes Cheese, Inc.

Recalled Item: Pasteurized Process Cheese Spread packaged under the following brands and...

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: 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: 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
DrugAugust 11, 2023· Baxter Healthcare Corporation

Recalled Item: Dianeal PD-2 Peritonial Dialysis Solution with 1.5% Dextrose Recalled by...

The Issue: Lack of Assurance of Sterility: Potential presence of leaks originating from...

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 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
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
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
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 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· 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
Medical DeviceAugust 10, 2023· Bard Peripheral Vascular Inc

Recalled Item: Bard Marquee Disposable Core Biopsy Instrument Kit Recalled by Bard...

The Issue: Diameter mismatch between coaxial and biopsy needle (cutting cannula) in...

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

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

Recalled Item: PDS Plus Antibacterial (polydioxanone) Suture Recalled by ETHICON, LLC Due...

The Issue: Internal testing on returned product from this lot confirmed that some PDS"...

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· ETHICON, LLC

Recalled Item: PDS II (polydioxanone) Suture Recalled by ETHICON, LLC Due to Internal...

The Issue: Internal testing on returned product from this lot confirmed that some PDS"...

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· ARROW INTERNATIONAL Inc.

Recalled Item: Arrow ErgoPack Recalled by ARROW INTERNATIONAL Inc. Due to This recall has...

The Issue: This recall has been initiated due to reports that the product code and...

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: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