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. 2,359 recalls have been distributed to Mississippi in the last 12 months.
Showing 46641–46660 of 49,744 recalls
Recalled Item: IMPAX CV Reporting Cardiac Catheterization module and IMPAX CV Outbound...
The Issue: Baseline pulmonary capillary wedge (PCW) pressure values from IMPAX CV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnesium Sulfate 2 grams in Dextrose 5% for Injection Recalled by Med Prep...
The Issue: Non-Sterility; mold contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All Compounded Products Recalled by Med Prep Consulting, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility; potential for mold contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Seasonale(R) (Levonorgestrel/Ethinyl Estradiol Tablets) Recalled by Teva...
The Issue: Failed Impurity/Degradation Specification; an impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Camrese(TM) (Levonorgestrel/Ethinyl Estradiol Tablets) Recalled by Teva...
The Issue: Failed Impurity/Degradation Specifications; an impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MUSCLEPHARM brand COMBAT POWDER (R) Recalled by F.H.G Corporation dba...
The Issue: One lot of each product may have extraneous materials due to a problem on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MUSCLEPHARM brand COMBAT POWDER (R) Recalled by F.H.G Corporation dba...
The Issue: One lot of each product may have extraneous materials due to a problem on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VITROS Chemistry Products PHBR (Phenobarbital) Slides Recalled by...
The Issue: Ortho Clinical Diagnostics (OCD) received customer complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Oxford Partial Knee Recalled by Synvasive Technology Inc Due to Biomet...
The Issue: Biomet part # 506076, lot 928182 was received from Synvasive Technology...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Duraflo coated Femoral Cannula. Product Usage: The...
The Issue: Two unsealed pouches were found at an Edwards' distribution location in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precise Treatment Table. To be used as part of radiation Recalled by Elekta,...
The Issue: The Column rotation can accidentally be moved to a different position which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunchang Ssamjang Sesame and Garlic Seasoned Bean Paste 500 g Recalled by...
The Issue: Sesame and Garlic Flavored Mixed Soy Bean Paste contains peanut powder which...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: epoc BGEM Test Card (Catalogue number CT-1004-00-00). quantitative testing...
The Issue: This recall is being initiated because the affected lots of this product may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE. Produce a monolayer of cells...
The Issue: Separation Technology, Inc. recalled SlidePrep Plus Cytology Centrifuges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rad-8 Pulse Oximeters The Rad-8 family of pulse oximeters and Recalled by...
The Issue: Masimo has identified a very small number (0.02%) of Rad-8 devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Vitamin D Assay (100 tests) Recalled by Siemens Healthcare...
The Issue: Negative bias in patient samples for Vitamin D
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Vitamin D Assay (500 tests) Recalled by Siemens Healthcare...
The Issue: Negative bias in patient samples for Vitamin D
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Vitamin D Calibrator 2-pack Recalled by Siemens Healthcare...
The Issue: Negative bias in patient samples for Vitamin D
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Vitamin D Calibrator 6-pack Recalled by Siemens Healthcare...
The Issue: Negative bias in patient samples for Vitamin D
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Archer 0.035 inch (0.89mm) Super Stiff Guidewire Recalled by...
The Issue: Medtronic has identified an issue involving specific lot numbers of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.