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. 2,476 recalls have been distributed to Mississippi in the last 12 months.
Showing 23561–23580 of 28,172 recalls
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Illumina Worklist Manager (IWM) (software v1.0.15) Recalled by Illumina Inc...
The Issue: A software component of the MiSeqDx instrument, called the Illumina Worklist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen...
The Issue: These lots of Agar may have exhibited breakthrough growth of vancomycin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RADIANCE v. 2.4X Recalled by Radiometer America Inc Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minstrel (with scale) Product Usage: is a mobile passive hoist. Recalled by...
The Issue: ArjoHuntleigh received three reports where the bolt under the scale...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Portal (ISP) DX/HX/EX Recalled by Philips Medical Systems...
The Issue: The following software issues have been identified in the affected products....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Battery 1 Model: TA-UB1 NSN: 6515-01-592-5803 The Ultra Battery...
The Issue: Estill has discovered that a fully discharged Ultra Battery 1 (TA-UB1) will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GALT VALVED TEARAWAY KIT GALT VTI w/ Sideport Stainless Steel Recalled by...
The Issue: The adhesive used in the product could dislodge when objects are inserted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GALT VALVED TEARAWAY INTRODUCER SET GALT VTI RX ONLY UNITS Recalled by Galt...
The Issue: The adhesive used in the product could dislodge when objects are inserted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL Sleeve Installation Tool Sizes: 6mm Recalled by OrthoPediatrics Corp Due...
The Issue: Weld fractures on the Sleeve Installation Tool for ACL reconstruction system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUN DASH RADIUS 252 PN 8000809705. The device is intended Recalled by JK...
The Issue: The integrity of the wires inside main electrical chord become compromised...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker T2 Tibia System Nail Insertion Sleeve Recalled by Stryker Howmedica...
The Issue: Stryker Orthopaedics received a report indicating some of the Nail Insertion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vl DBL OFFST WI LRG STPL Recalled by Zimmer, Inc. Due to The firm received...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VER2 D8L OFFSET RASP HANDLE Recalled by Zimmer, Inc. Due to The firm...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VER2 HANDLE Recalled by Zimmer, Inc. Due to The firm received complaints for...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VER2 HANDLE Recalled by Zimmer, Inc. Due to The firm received complaints for...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 23.5 Deg Rasp Handle Assy- LEFT Nonsterile Recalled by Zimmer, Inc. Due to...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.