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. 2,506 recalls have been distributed to Louisiana in the last 12 months.
Showing 25341–25360 of 29,201 recalls
Recalled Item: INOmax DSIR Recalled by INO Therapeutics (dba Ikaria) Due to An anomaly...
The Issue: An anomaly impacts the monitoring system of INOmax DSIR Plus (software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ToxCup Drug Screen Cup Recalled by Branan Medical Corporation Due to May be...
The Issue: May be labeled with incorrect result interpretation graphics on the ToxCup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Acumed Tension Band Pin is a fixation pin which Recalled by Acumed LLC...
The Issue: Certain lots of Acumed Tension Band Pins are being recalled because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Osteo-Clage System consists of stainless steel cable/sleeves and...
The Issue: Manufacturing of these devices with a grade of stainless steel that is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker PenAdapt" Recalled by Stryker Instruments Div. of Stryker...
The Issue: During packaging verification testing, a failure occurred due to cuts in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products FS Diluent Pack 3 Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics (OCD) confirmed the potential for lower than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Specialty Diluent Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics (OCD) confirmed the potential for lower than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlloFuse DBM Putty 5cc Recalled by AlloSource, Inc. Due to The donor was...
The Issue: The donor was hemodiluted.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...
The Issue: The Tyvek cover may not be completely sealed to the rest of the package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...
The Issue: The Tyvek cover may not be completely sealed to the rest of the package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...
The Issue: The Tyvek cover may not be completely sealed to the rest of the package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...
The Issue: The Tyvek cover may not be completely sealed to the rest of the package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable latex breathing bags with multiple part numbers and sold Recalled...
The Issue: Reusable latex breathing bags with various part numbers and sold as part of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Folate Cat No. 06891541 SMN 10325366 (500 Recalled by...
The Issue: Serum controls may go out of range low with the ADVIA Centaur ¿Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...
The Issue: The Tyvek cover may not be completely sealed to the rest of the package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AxoTrack I Sterile Procedure Kit 18G Recalled by Soma Access Systems LLC Due...
The Issue: There is a possibility the sterile packaging may fail before the expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Pressure Injectable PICC Powered by Arrow VPS Stylet Catalogue...
The Issue: Kits are packaged with the incorrect catheter. The kits contain a 40cm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Emotion 16 Recalled by Siemens Medical Solutions USA, Inc...
The Issue: The rubber damper may degrade and break, causing loosening of the motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope System 98/98xt Recalled by Maquet Datascope Corp - Cardiac Assist...
The Issue: Potential mechanical failure of the fan assembly associated with the power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 15FR Drain Kit Round End Perforated with Trocar and 100ml S-Vac Bulb...
The Issue: The recall has been initiated due to a potential compromise of the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.