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. 2,683 recalls have been distributed to Louisiana in the last 12 months.
Showing 6801–6820 of 29,201 recalls
Recalled Item: Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device...
The Issue: Problem maintaining the stable placement of the battery may come loose from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iradimed Corporation MRidium MRI 1000 Series Infusion Sets Recalled by...
The Issue: Certain Iradimed 1057 Syringe Adapter Sets, used with the MRidium MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only and Recalled by...
The Issue: Mislabeled: Product is marked with GTIN # 04046955299592 however; the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Rotatable Clip Fixing Device Model HX 201LR 135 - Rotatable...
The Issue: There have been complaints that the clip did not come out of the tube sheath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus Pro Patient Monitor is a portable vital signs monitor Recalled by...
The Issue: During internal testing, Regulatory Compliance issues were identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to Bio-Rad received...
The Issue: Bio-Rad received four customer complaints from 11/30/2022 to 12/21/2022 on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to Bio-Rad received...
The Issue: Bio-Rad received four customer complaints from 11/30/2022 to 12/21/2022 on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath Recalled by...
The Issue: Incorrect labeling; specifically, the product name, lot number and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath Recalled by...
The Issue: Incorrect labeling; specifically, the product name, lot number and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Lysis Beads Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent GM X 6mm Engaging Titanium Base Recalled by Preat Corp Due to...
The Issue: Engaging titanium base contains a dimensional condition that allows vertical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent RVD with RVD Enhancer: a) 1 mL Recalled by Entopsis , Inc....
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis BCSNano (1mL) Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Support: a) 1 mL Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent RVD-RT Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Activator: a) 1.5mL Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent Buccal Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPerfusion Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: There are technical issues related to signal generation and processing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2D Perfusion Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to There...
The Issue: There are technical issues related to signal generation and processing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moberg Component Neuromonitoring System (CNS Monitor)-Intended as a...
The Issue: Battery leakage can cause corrosion to the metal enclosure near the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.