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. 2,523 recalls have been distributed to Louisiana in the last 12 months.
Showing 23301–23320 of 51,202 recalls
Recalled Item: Ally Bone Screw - Product Usage:Bone Screws are indicated for Recalled by...
The Issue: There may be dimensional manufacturing error that represents a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestilix 1600X Prestilix system is a fully integrated remote controlled...
The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestige II Recalled by GE Healthcare, LLC Due to There has been a reported...
The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Silhouette VR This fully integrated system offers intuitive controls with...
The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus XR/a The Proteus XR/a radiographic system offers the flexibility...
The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conformis iTotal Hip Replacement System: HBS-033-00xx-020101 Recalled by...
The Issue: Discrepancy of 3mm between the values displayed and approved by surgeons in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precision 500D The Precision 500D R&F X-ray System is intended Recalled by...
The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Nail Clipper Concave Edge (67710) Recalled by Centurion Medical...
The Issue: Compromised seal on the sterile barrier pouch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Nail Nipper Recalled by Centurion Medical Products Corporation Due...
The Issue: Compromised seal on the sterile barrier pouch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Jubilant Cadista...
The Issue: Discoloration: Expansion of an earlier recall due to the presence of dark...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clonidine HCL Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...
The Issue: Labeling: Label Error on Declared Strength: Side carton panel incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Recalled...
The Issue: There is a potential of fracture, bending or shearing of the driver.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...
The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...
The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T7 Driver Solid AO (Part Number 110018541) Product Usage: The Recalled by...
The Issue: There is a potential of fracture, bending or shearing of the driver.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Yellow Corn Flour #620 Recalled by Iowa Corn Processors Due to Foreign...
The Issue: Product could contain foreign objects (pliable blue plastic)
Recommended Action: Do not consume. Return to store for a refund or discard.