Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,623 recalls have been distributed to Mississippi in the last 12 months.
Showing 7841–7860 of 49,744 recalls
Recalled Item: 2008T HD SYS. CDX W/BIBAG BLUESTAR Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T Hemodialysis System without CDX Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis CII Safe ES Recalled by CareFusion 303, Inc. Due to When global...
The Issue: When global edit is used to update multiple formulary properties...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HD SYS. CDX BLUESTAR Recalled by Fresenius Medical Care Holdings, Inc....
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venue Go Standard Carts Ref: (H45181VC and H45103VCW) Recalled by GE MEDICAL...
The Issue: Some Venue Go Standard Carts can develop an internal failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meera Mobile Operating Table-to support and position the patient immediately...
The Issue: Under certain conditions, an issue might prevent the device from performing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pantoprazole Sodium for Injection 40mg per vial Recalled by BE...
The Issue: Lack of Assurance of Sterility: Powder discoloration due to small crack in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MAZOR X robotic guidance system Recalled by Mazor Robotics Ltd Due to...
The Issue: Software update
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dermatome Blades- 10-pack boxes of blades. Intended for use Recalled...
The Issue: Skin grafts thin and non-uniform when using the affected blades. The issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydrALAZINE Hydrochloride Tablets Recalled by Amerisource Health Services...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ethos Collar Stem Recalled by Onkos Surgical, Inc. Due to Potential for...
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. Segmental Stem Recalled by Onkos Surgical, Inc. Due to Potential for...
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental Stem Recalled by Onkos Surgical, Inc. Due to Potential for breach...
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental Stem Recalled by Onkos Surgical, Inc. Due to Potential for breach...
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Male-Female Midsection with the following sizes and model numbers. a....
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental Stem Recalled by Onkos Surgical, Inc. Due to Potential for breach...
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: The Guardian System Product Name: The Guardian Model/Catalog...
The Issue: Device reaching End of Service prematurely.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solea Models 2.0 and 3.0 Laser Surgical Instrument Recalled by Convergent...
The Issue: It has been found that potential unintended laser activation can occur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAVH Recalled by American Contract Systems, Inc. Due to During an internal...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Robotics Pack SAH Recalled by American Contract Systems, Inc. Due to During...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.