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. 2,492 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,492 in last 12 months

Showing 2696126980 of 52,000 recalls

DrugMay 17, 2018· Shoreside Enterprises Inc.

Recalled Item: POSEIDON Xtreme PLATINUM 4500 Recalled by Shoreside Enterprises Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found products to...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 17, 2018· Lupin Pharmaceuticals Inc.

Recalled Item: My Way (Levonorgestrel) Tablets TWO PACK Recalled by Lupin Pharmaceuticals...

The Issue: Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 17, 2018· Lupin Pharmaceuticals Inc.

Recalled Item: My Way (levonorgestrel) Tablets TWO PACK Recalled by Lupin Pharmaceuticals...

The Issue: Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2018· Ideaz Llc

Recalled Item: screamin' menthol (menthol) Pain Relieving Gel Recalled by Ideaz Llc Due to...

The Issue: CGMP Deviations: Products manufactured with an ingredient that exceed the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2018· Ideaz Llc

Recalled Item: screamin' hot (capsaicin) Pain Relieving Gel Recalled by Ideaz Llc Due to...

The Issue: CGMP Deviations: Products manufactured with an ingredient that exceed the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2018· Inopak Ltd

Recalled Item: Option Systems Antibacterial Foaming Hand Wash with .3% PCMX Recalled by...

The Issue: Microbial contamination of NonSterile Product; FDA analysis returned out of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2018· Nature's Only Choice

Recalled Item: Nature's Only Choice B17 BITTER RAW APRICOT EXTRACT AMYGDALIN Dietary...

The Issue: The Vitamin B17 containing product is considered to be a prescription drug,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Immunoglobulin A is an in vitro diagnostic assay for the Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Apolipoprotein A1 is an in vitro diagnostic assay for the Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: C4 is an in vitro diagnostic assay for the quantitative Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Immunoglobulin G is an in vitro diagnostic assay for the Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Apolipoprotein B is an in vitro diagnostic assay for the Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Transferrin is an in vitro diagnostic assay for the quantitative Recalled by...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: C3 is an in vitro diagnostic assay for the quantitative Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: The Recalled by Abbott Laboratories, Inc Due to An update to the Reagents...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Immunoglobulin M is an in vitro diagnostic assay for the Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: 3.2MM X 510MM COCR THD TIP Recalled by Zimmer Biomet, Inc. Due to The firm...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: RECON DRILL 6MM X 439MM Recalled by Zimmer Biomet, Inc. Due to The firm is...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: BALL TIP GUIDE WIRE 3.2MMX98CM Recalled by Zimmer Biomet, Inc. Due to The...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: BALL TIP GUIDE WIRE 3.2MMX55CM Recalled by Zimmer Biomet, Inc. Due to The...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing