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. 1,021 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
1,021 in last 12 months

Showing 19741–19760 of 51,202 recalls

Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Set Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: 10 cc Luer-Slip Loss of Resistance Syringe Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Bard Peripheral Vascular Inc

Recalled Item: BARD Access Systems PowerPort ClearVUE Slim Implantable Port With Smooth...

The Issue: The catheter locks for the lot may contain an 8Fr catheter lock instead of a...

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

Class II — Potential Health HazardOngoing
FoodJanuary 15, 2020· The Honest Stand

Recalled Item: Hungry Root Dairy free Garlic Parm sauce Recalled by The Honest Stand Due to...

The Issue: Undeclared Allergen: Product contains both cashews and almonds, but only...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 15, 2020· Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Recalled Item: Methylprednisolone Acetate Injectable Suspension Recalled by Fusion IV...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2020· Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Recalled Item: Glycine Injection Recalled by Fusion IV Pharmaceuticals, Inc. dba Axia...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2020· Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Recalled Item: Alprostadil/Papaverine Hydrochloride/Phentolamine Mesylate Injection...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2020· Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Recalled Item: Alprostadil (prostaglandin E1) 80 MCG/ML Injectable Recalled by Fusion IV...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2020· Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Recalled Item: BETAMETHASONE ACETATE/BETAMETHASONE (PF) Injectable Suspension Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2020· Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Recalled Item: Glutathione Injection Recalled by Fusion IV Pharmaceuticals, Inc. dba Axia...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2020· Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Recalled Item: Polyoxyl Lauryl Ether (Polidocanol) Injection Recalled by Fusion IV...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2020· Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Recalled Item: AscorbiX (Buffered C) Injection Recalled by Fusion IV Pharmaceuticals, Inc....

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2020· Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Recalled Item: Selenium Injection Recalled by Fusion IV Pharmaceuticals, Inc. dba Axia...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 14, 2020· Pharmaceutical Associates Inc

Recalled Item: Nystatin Oral Suspension Recalled by Pharmaceutical Associates Inc Due to...

The Issue: Subpotent: Out of specification for assay at the 12-month time point.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 14, 2020· Hikma Pharmaceuticals USA Inc.

Recalled Item: methylPREDNISolone Sodium Succinate For Injection Recalled by Hikma...

The Issue: Labeling: Incorrect Instructions: Vial label incorrectly instructs...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 14, 2020· Abbott Point Of Care Inc.

Recalled Item: i-STAT G3+ cartridge (blue) Recalled by Abbott Point Of Care Inc. Due to...

The Issue: Marketed without a 510(k). Abbott Point of Care has determined that it does...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2020· Ormco/Sybronendo

Recalled Item: Ormco Damon Q2 Orthodontic Metal Bracket Recalled by Ormco/Sybronendo Due to...

The Issue: The bracket torque was mislabeled on the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2020· CME America, LLC

Recalled Item: BodyGuard Microset For Use with the BodyGuard Infusion Pump *** Recalled by...

The Issue: The filter installed onto the tube set may have the incorrect pore size.

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

Class II — Potential Health HazardOngoing