Product Recalls in Louisiana

Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,807 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
1,807 in last 12 months

Showing 3438134400 of 51,202 recalls

Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.) Recalled...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Pediatric ThermoGard¿ Dual Dispersive Electrodes (for patients 5-15 kg.)...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.) Recalled...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Adult Dual Dispersive Electrodes (for patients >15 kg.) Recalled by Conmed...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Pediatric Dual Dispersive Electrodes (for patients 5-15 kg.) Recalled by...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Ca Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics (OCD) confirmed a potential for biased calcium...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Elekta, Inc.

Recalled Item: Monaco RTP System Product Usage: The Monaco system is used Recalled by...

The Issue: When DICOM exporting a 3D Monaco plan and the "Composite Field Sequencing"...

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

Class II — Potential Health HazardOngoing
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Akorn, Inc.

Recalled Item: Sulfacetamide Sodium Ophthalmic Solution Recalled by Akorn, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility; some lots failed Antimicrobial Effectiveness...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 17, 2016· X Spine Systems Inc

Recalled Item: Calix T PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...

The Issue: The trials and rasps used to prepare the surgical site for placement of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2016· X Spine Systems Inc

Recalled Item: Calix P PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...

The Issue: The trials and rasps used to prepare the surgical site for placement of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2016· X Spine Systems Inc

Recalled Item: Calix P PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...

The Issue: The trials and rasps used to prepare the surgical site for placement of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2016· X Spine Systems Inc

Recalled Item: Calix T PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...

The Issue: The trials and rasps used to prepare the surgical site for placement of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2016· CSL Behring GmbH

Recalled Item: Dimension Vista¿ Homocysteine Flex Reagent Cartridge (HCYS) Recalled by CSL...

The Issue: Reagent lots # 15243MA and 15243MB shows a reduced stability once opened...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2016· Roche Molecular Systems, Inc.

Recalled Item: cobas¿ Liat Influenza A/B Quality Control Kit Recalled by Roche Molecular...

The Issue: Kit labeled with the incorrect expiration date.

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

Class III — Low RiskOngoing