Product Recalls in Mississippi

Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,394 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,394 in last 12 months

Showing 4298143000 of 49,744 recalls

Medical DeviceFebruary 3, 2014· Hospira Inc.

Recalled Item: The GemStar Power Supply is an accessory for the GemStar Recalled by Hospira...

The Issue: The GemStar Infusion pump may not receive direct current (DC) power from the...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 3, 2014· Hospira Inc.

Recalled Item: The GemStar Power Supply is an accessory for the GemStar Recalled by Hospira...

The Issue: The GemStar Infusion pump may not receive direct current (DC) power from the...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 3, 2014· Altasource LLC dba Meta Labs LLC

Recalled Item: Hot Ice Recalled by Altasource LLC dba Meta Labs LLC Due to Firm is not...

The Issue: Firm is not registered as a drug manufacturer.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Altasource LLC dba Meta Labs LLC

Recalled Item: Nice-En-Smooth Berry Burst Recalled by Altasource LLC dba Meta Labs LLC Due...

The Issue: Firm is not registered as a drug manufacturer.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Altasource LLC dba Meta Labs LLC

Recalled Item: Amo-O Herbal Stimulator Recalled by Altasource LLC dba Meta Labs LLC Due to...

The Issue: Firm is not registered as a drug manufacturer.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Altasource LLC dba Meta Labs LLC

Recalled Item: Mega-Gen His Personal Lubricant Recalled by Altasource LLC dba Meta Labs LLC...

The Issue: Firm is not registered as a drug manufacturer.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Stryker Howmedica Osteonics Corp.

Recalled Item: Citation TMZF HA 132 degrees Neck Angle Recalled by Stryker Howmedica...

The Issue: Stryker received a report from the field indicating that a citation TMZF HA...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Siemens Medical Solutions Diagnostics

Recalled Item: IMMULITE 2000 Recalled by Siemens Medical Solutions Diagnostics Due to There...

The Issue: There is a potential for incorrect results to be reported from processing of...

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

Class II — Potential Health HazardOngoing
DrugJanuary 31, 2014· American Health Packaging

Recalled Item: HydrOXYzine HCl Tablets Recalled by American Health Packaging Due to Good...

The Issue: Good Manufacturing Practices Deviations: The product has an active...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 31, 2014· American Health Packaging

Recalled Item: HydrOXYzine HCl Tablets Recalled by American Health Packaging Due to Good...

The Issue: Good Manufacturing Practices Deviations: The product has an active...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: SETON PHARMACEUTICALS Fluocinolone acetonide 0.01% Topical Oil (Scalp Oil)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Body Oil) 4 fl....

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01% Oil EAR DROPS Recalled by...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: ROYAL PHARMACEUTICALS DermOtic Oil fluocinolone acetonide 0.01% (Ear Drops)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

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

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: DermOtic Oil (fluocinolone acetonide) 0.01% Ear Drops Recalled by Hill...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: ROYAL PHARMACEUTICALS Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01% Topical Oil (Body Oil)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: ROYAL PHARMACEUTICALS Derma-Smoothe/FS fluocinolone acetonide 0.01% (Scalp...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 31, 2014· Hospira Inc.

Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to The connection between...

The Issue: The connection between the beeper subassembly and the pump may fail. The...

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

Class II — Potential Health HazardOngoing