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. 2,678 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,678 in last 12 months

Showing 81818200 of 51,202 recalls

Medical DeviceAugust 10, 2023· Bard Peripheral Vascular Inc

Recalled Item: Bard Marquee Disposable Core Biopsy Instrument Kit Recalled by Bard...

The Issue: Diameter mismatch between coaxial and biopsy needle (cutting cannula) in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Epiphany Cardio Server E3 ECG Management System Servers with Recalled...

The Issue: Epiphany, now a Baxter Healthcare company, is issuing an Urgent Medical...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· ARROW INTERNATIONAL Inc.

Recalled Item: Arrow ErgoPack Pressure Injectable One-Lumen PICC Recalled by ARROW...

The Issue: This recall has been initiated due to reports that the product code and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· ARROW INTERNATIONAL Inc.

Recalled Item: Arrow ErgoPack Recalled by ARROW INTERNATIONAL Inc. Due to This recall has...

The Issue: This recall has been initiated due to reports that the product code and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· ETHICON, LLC

Recalled Item: PDS Plus Antibacterial (polydioxanone) Suture Recalled by ETHICON, LLC Due...

The Issue: Internal testing on returned product from this lot confirmed that some PDS"...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· ETHICON, LLC

Recalled Item: PDS II (polydioxanone) Suture Recalled by ETHICON, LLC Due to Internal...

The Issue: Internal testing on returned product from this lot confirmed that some PDS"...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Baxter Healthcare Corporation

Recalled Item: Welch Allyn Connex Spot Monitor Recalled by Baxter Healthcare Corporation...

The Issue: Product is being recalled due to the improper placement of a copper tape on...

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

Class II — Potential Health HazardOngoing
DrugAugust 9, 2023· Ecometics, Inc.

Recalled Item: activator concentrate Recalled by Ecometics, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2023· Ecometics, Inc.

Recalled Item: Lugol's (Strong Iodine Solution USP) Recalled by Ecometics, Inc. Due to CGMP...

The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2023· Ecometics, Inc.

Recalled Item: AstrinGyn (Ferric Subsulfate) Aqueous Recalled by Ecometics, Inc. Due to...

The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2023· Ecometics, Inc.

Recalled Item: ALCOLADO RELAMPAGO (Menthol and Camphor) Recalled by Ecometics, Inc. Due to...

The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2023· Ecometics, Inc.

Recalled Item: Blis-To-Sol Liquid (Tolnaftate) Recalled by Ecometics, Inc. Due to CGMP...

The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2023· Ecometics, Inc.

Recalled Item: Unguentine Ointment Recalled by Ecometics, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2023· Ecometics, Inc.

Recalled Item: YAGER'S LINIMENT (Camphor and Turpentine Oil) 3.1% and 8.12% respectively...

The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 9, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Proboscis/Piston Assembly Recalled by Ortho-Clinical Diagnostics, Inc. Due...

The Issue: Ortho Clinical Diagnostics (QuidelOrtho) confirmed certain Proboscis/Piston...

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

Class II — Potential Health HazardOngoing
FoodAugust 8, 2023· Bickel's Snack Foods Inc

Recalled Item: Butter Flavored Popcorn Naturally & Artificially Flavored Recalled by...

The Issue: Undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 8, 2023· FX SHOULDER

Recalled Item: Centered Glenosphere w/Screw Recalled by FX SHOULDER Due to Centered...

The Issue: Centered glenosphere box may contain an eccentric glenosphere.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 3ML Syringe Luer Lock with needle 20GX1 Recalled by Fresenius Medical Care...

The Issue: There is a potential for blood backfill leakage and foreign material.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 8, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 10ML SYRINGE LUER LOCK W/NEEDLE Recalled by Fresenius Medical Care Holdings,...

The Issue: There is a potential for blood backfill leakage and foreign material.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 8, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 10ML SYRINGE LUER LOCK W/OUT NEEDLE Recalled by Fresenius Medical Care...

The Issue: There is a potential for blood backfill leakage and foreign material.

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

Class I — Serious Health HazardOngoing