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. 2,635 recalls have been distributed to Mississippi in the last 12 months.
Showing 6141–6160 of 28,172 recalls
Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EliA GBM Wells Recalled by Phadia Ab Due to Complaints that specific samples...
The Issue: Complaints that specific samples produced false positive EliA GBM results. A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuMoDx Cartridge-used for extraction Recalled by NeuMoDx Molecular Inc Due...
The Issue: Top label on some of the NeuMoDx cartridges within these lots may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RET Distal Probe. Used in Fluorescence in situ hybridization (FISH) Recalled...
The Issue: DNAs used during the manufacture of two affected models were accidentally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RET Proximal Probe. Used in Fluorescence in situ hybridization (FISH)...
The Issue: DNAs used during the manufacture of two affected models were accidentally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-PRO 2- A powered ambulance cot that consists of a platform Recalled by...
The Issue: Base leg assembly may bend and result in difficulty engaging/disengaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Sterile CirClamp with 1.45cm Bell Reprocessed Recalled by MEDLINE...
The Issue: The kits incorrectly contain CirClamp subassembly 345CRSAK which results in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PriMatrix Ag Meshed Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend PRS Meshed Recalled by TEI Biosciences, Inc. Due to Possible out...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend 3.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend 1.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PriMatrix Fenestrated Recalled by TEI Biosciences, Inc. Due to Possible out...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PriMatrix Ag Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PriMatrix Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PriMatrix Ag Fenestrated Recalled by TEI Biosciences, Inc. Due to Possible...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revize Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revize-X Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.