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. 2,638 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,638 in last 12 months

Showing 1338113400 of 13,463 recalls

DrugMay 18, 2012· InSo-Independent Contractor for West Coast Nutritionals,LTD

Recalled Item: a) Firminite 805 mg is packaged in 2 count Recalled by InSo-Independent...

The Issue: Marketed Without an Approved NDA/ANDA: These products found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 17, 2012· Mcneil Consumer Healthcare, Div Of Mcneil-ppc, Inc.

Recalled Item: Imodium Multi-Symptom Relief Caplets Recalled by Mcneil Consumer Healthcare,...

The Issue: Defective Container; damaged blister units

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

Class III — Low RiskOngoing
Refund
DrugMay 14, 2012· Abbott Laboratories

Recalled Item: Zemplar (paricalcitol) Injection Recalled by Abbott Laboratories Due to CGMP...

The Issue: CGMP Deviations: There is potential that Abbott's third party manufacturer,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2012· Hospira Inc.

Recalled Item: HYDROmorphone HCl Injection Recalled by Hospira Inc. Due to Superpotent...

The Issue: Superpotent (Single Ingredient) Drug: Some of the prefilled cartridge units...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 9, 2012· Grandpa Brands Co

Recalled Item: Dent's Extra Strength Toothache Gum Recalled by Grandpa Brands Co Due to...

The Issue: Superpotent; benzocaine

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 8, 2012· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (Fluocinolone Acetonide) 0.01% Topical Oil (Scalp Oil)...

The Issue: Subpotent; fluocinolone acetonide

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

Class III — Low RiskOngoing
Refund
DrugMay 8, 2012· Morton Salt Co.

Recalled Item: Morton Recalled by Morton Salt Co. Due to Impurities/Degradation Products:...

The Issue: Impurities/Degradation Products: The product was found to contain a slightly...

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

Class III — Low RiskOngoing
Refund
DrugMay 8, 2012· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (Fluocinolone Acetonide) 0.01% Recalled by Hill...

The Issue: Subpotent; fluocinolone acetonide

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Endo Pharmaceuticals, Inc.

Recalled Item: Endocet (oxycodone and acetaminophen) tablets Recalled by Endo...

The Issue: Adulterated Presence of Foreign Tablets: Customer complaint that some...

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 5% Dextrose Injection USP Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 1.5% Glycine Irrigation Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 5% Dextrose and 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 70% Dextrose Injection USP Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund