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. 1,061 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
1,061 in last 12 months

Showing 14501–14520 of 51,202 recalls

FoodOctober 29, 2021· Puratos Corporation (HQ and Innovation Center)

Recalled Item: One Step Neutral/Vanilla Mousse Bag 25#. Material #4107486 Recalled by...

The Issue: Product may be contaminated with foreign material (metal)

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 29, 2021· NuVasive Specialized Orthopedics, Inc.

Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System:...

The Issue: The Instructions for Use have been updated to include: (1) Clarification...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2021· Diversatek Healthcare

Recalled Item: Diversatek Health Recalled by Diversatek Healthcare Due to M-Catch Retrieval...

The Issue: M-Catch Retrieval Nets, Part Number 1175-01 / Lot Number 001919, that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2021· Philips North America Llc

Recalled Item: Wireless Footswtich used with the following Philips Allura Xper and Recalled...

The Issue: Wireless foot switch connection issues causing interruption of Fluoroscopy...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2021· Osteomed, LLC

Recalled Item: OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 by...

The Issue: Due to consoles not in compliance with the latest electrical safety...

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

Class II — Potential Health HazardOngoing
FoodOctober 28, 2021· MARY RUTH ORGANICS

Recalled Item: MaryRuth's Organic Infants Liquid Probiotic Recalled by MARY RUTH ORGANICS...

The Issue: Internal testing found the presence of Pseudomonas aeruginosa in the product.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 28, 2021· Palodex Group Oy

Recalled Item: Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray...

The Issue: It was noticed in production on 28.10.2021, that the final testing database...

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

Class II — Potential Health HazardOngoing
DrugOctober 28, 2021· Teva Pharmaceuticals USA

Recalled Item: Clonidine Transdermal System Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugOctober 27, 2021· Teva Pharmaceuticals USA

Recalled Item: Cartia XT (Diltiazem Hydrochloride Extended-Release Capsules Recalled by...

The Issue: Labelling: Incorrect Exp. Date

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Venous Access Pack-LF Convenience Kit Recalled by Medline Industries Inc Due...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: EVLP Convenience Pack/Kit Recalled by Medline Industries Inc Due to NaCl 250...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Major Vascular CDS Convenience Kit Recalled by Medline Industries Inc Due to...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Neuro Convenience Kit Recalled by Medline Industries Inc Due to NaCl 250 mL...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Bedside PICC CDS Convenience Kit Recalled by Medline Industries Inc Due to...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2021· MAX LUX CORP

Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...

The Issue: Excessive ultraviolet-C radiation

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

Class II — Potential Health HazardOngoing
DrugOctober 26, 2021· Perrigo Company PLC

Recalled Item: Acetaminophen Child Dye Free Cherry Flavor Oral Suspension (160mg/5ml)...

The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2021· Perrigo Company PLC

Recalled Item: Maximum Strength No Drip Nasal Spray Recalled by Perrigo Company PLC Due to...

The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2021· Perrigo Company PLC

Recalled Item: Acetaminophen Child Strawberry Oral Suspension (160 mg/5 ml) Recalled by...

The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2021· Perrigo Company PLC

Recalled Item: Severe Congestion No Drip Nasal Spray Plus Menthol Recalled by Perrigo...

The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2021· Perrigo Company PLC

Recalled Item: Maximum Strength No Drip Nasal Spray Recalled by Perrigo Company PLC Due to...

The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...

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

Class II — Potential Health HazardOngoing
Refund