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. 2,661 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,661 in last 12 months

Showing 1210112120 of 13,463 recalls

DrugJuly 12, 2013· Hospira Inc.

Recalled Item: 0.25% Bupivacaine HCl Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of particulate matter: visible free floating and partially embedded...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 4, 2013· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to Failed...

The Issue: Failed Impurites/Degradation Specifications: Test failure of single largest...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 3, 2013· Procter & Gamble Co

Recalled Item: DayQuil Sinex DayTime Sinus Relief (acetaminophen 325 mg and phenylephrine...

The Issue: Unit Dose Mispackaging: Product packaging defect which could result in code...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2013· Core Pharma Llc

Recalled Item: Pyridostigmine Bromide Tablets 60 mg Recalled by Core Pharma Llc Due to...

The Issue: Failed Stability Specifications: Pyridostigmine Bromide tablets, is being...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 1, 2013· Fresenius Kabi USA, LLC

Recalled Item: Benztropine Mesylate Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Presence of particulate matter: characterized as thin colorless flakes that...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 400 ec Recalled by Stayma Consulting Service, LLC. Due to...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 430 Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: NataChew Recalled by Stayma Consulting Service, LLC. Due to Subpotent; Beta...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Nata Komplete Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 400 Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA Balanced Recalled by Stayma Consulting Service, LLC. Due to...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 430 ec Recalled by Stayma Consulting Service, LLC. Due to...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2013· Max Huber Research Labs, Inc.

Recalled Item: LA MER the spf 18 fluid tint Recalled by Max Huber Research Labs, Inc. Due...

The Issue: Subpotent Drug: Avobenzone 3%, one of the active sunscreen ingredients may...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2013· Max Huber Research Labs, Inc.

Recalled Item: LA MER the spf 18 fluid tint Recalled by Max Huber Research Labs, Inc. Due...

The Issue: Subpotent Drug: Avobenzone 3%, one of the active sunscreen ingredients may...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2013· Hospira Inc.

Recalled Item: Sodium Chloride Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Confirmed customer report of visible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2013· Max Huber Research Labs, Inc.

Recalled Item: LA MER the spf 18 fluid tint Recalled by Max Huber Research Labs, Inc. Due...

The Issue: Subpotent drug: Avobenzone 3%, one of the active sunscreen ingredients may...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2013· Fabscout Entertainment, Inc

Recalled Item: Silver Sword capsules Recalled by Fabscout Entertainment, Inc Due to...

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 27, 2013· Fabscout Entertainment, Inc

Recalled Item: Clalis capsules Recalled by Fabscout Entertainment, Inc Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 25, 2013· Apotex Inc

Recalled Item: Latanoprost Ophthalmic Solution Recalled by Apotex Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: Failed at expiry for Preservative...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 24, 2013· Fresenius Kabi USA, LLC

Recalled Item: Oxytocin Injection Recalled by Fresenius Kabi USA, LLC Due to Subpotent...

The Issue: Subpotent Drug; 15-month stability test station

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

Class II — Potential Health HazardOngoing
Refund