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. 2,496 recalls have been distributed to Louisiana in the last 12 months.
Showing 33141–33160 of 51,202 recalls
Recalled Item: Brivo XR385 Recalled by GE Healthcare, LLC Due to The placing of weight on...
The Issue: The placing of weight on the VRAD detector, of the Brivo XR385 digital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 5ml Syringe Luer-Lok" Tip with Blunt Fill Needle 18G Recalled by Becton...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xanax (Alprazolam) USP Recalled by Mckesson Packaging Services Due to...
The Issue: Labeling: Missing Label-Primary packaging label (i.e. blister card) is blank...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PREMARIN (conjugated estrogen tablets Recalled by Pfizer Inc. Due to...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Bottles were incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dimension Vista Chemistry 1 Calibrator The Chemistry 1 Calibrator (KC110B)...
The Issue: Siemens determined that discrepant low calcium recovery of QC and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Synapse PACS Recalled by Fujifilm Medical Systems U.S.A., Inc. Due...
The Issue: Image data for a patients image may not be correct
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keystone Dental PrimaConnex¿ Straight Implant TC Recalled by Keystone Dental...
The Issue: Small diameter (SD) cover screw was packaged with the regular diameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SDMS (SenTec Digital Monitoring System) Recalled by SenTec AG Due to Sentec...
The Issue: Sentec AG found that with one batch of an internal SenTec Monitor component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agee-WristJack¿ Fracture Reduction System Recalled by Hand Biomechanics Lab...
The Issue: A number of Agee WristJack¿ Fracture Reduction Systems have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US...
The Issue: Customers complained of low/empty reagent vials.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LipiFlow thermal Pulsation System Recalled by Tearscience, Inc Due to...
The Issue: Complaints related to an error condition occurring during patient treatment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-release Tablets Recalled by Sun...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: mitoXANTRONE Injection USP (concentrate) Recalled by Teva Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: potential failure to meet the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Safecor Vitamin B-1 (THIAMINE) 100 mg tablets NDC: 48433-0108-01 Distributed...
The Issue: Box labeled Thiamine Hydrochloride instead of Thiamine Mononitrate
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Liquid VITAMIN D-3 Drops distributed under the following private labels...
The Issue: The lots exceed the label claim for Vitamin D3 of 2000 IU per drop.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cytotec (misoprostol) Tablets Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Impurities/Degradations Specifications; Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zero-Gravity Radiation Protection System Radiology Personnel protective...
The Issue: Two customer complaints suggest that excessive rotation of the cable in one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlucaGen HypoKit (glucagon [rDNA origin] for injection) Recalled by Novo...
The Issue: Defective delivery system: detached needles on the syringe in the kit.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Capsules Recalled by Mckesson Packaging...
The Issue: Labeling: Label mix-up. The inner packaging was properly labeled Omeprazole...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.