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. 1,734 recalls have been distributed to Mississippi in the last 12 months.
Showing 45861–45880 of 49,744 recalls
Recalled Item: Lipotonix Plus w/Proc/Chrom Recalled by Main Street Family Pharmacy, LLC Due...
The Issue: The firm received seven reports of adverse reactions in the form of skin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: B-12 0.5ml prefilled syringe Recalled by Main Street Family Pharmacy, LLC...
The Issue: The firm received seven reports of adverse reactions in the form of skin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HCG 290 iu prefilled syringes Recalled by Main Street Family Pharmacy, LLC...
The Issue: The firm received seven reports of adverse reactions in the form of skin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bacteriostatic Water 30ml Recalled by Main Street Family Pharmacy, LLC Due...
The Issue: The firm received seven reports of adverse reactions in the form of skin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HCG 7000u Recalled by Main Street Family Pharmacy, LLC Due to The firm...
The Issue: The firm received seven reports of adverse reactions in the form of skin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Actiq (oral transmucosal fentanyl citrate) 200 mcg Recalled by Teva...
The Issue: Failed Dissolution Specification; during stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eyebright Concentrate Topical Eye Rinse Recalled by Earthlabs, Inc. DBA Wise...
The Issue: Lack of Assurance of Sterility; Lack of Assurance of Sterility; product not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter; single visible particulate was identified...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magnesium Sulfate Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of Particulate Matter: Glass particulate matter was observed in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VIA Medical Collection Bag Recalled by International Biomedical, Ltd. Due to...
The Issue: International Biomedical has received reports of interference between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Service Replacement 0-Ring. Used in as a service part Recalled by...
The Issue: Incorrect rubber nitrile O-rings distributed instead of the correct material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GYRUS ACMI Recalled by Gyrus Acmi, Incorporated Due to lack of sterility...
The Issue: lack of sterility assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMICUS Exchange Kit Recalled by Fenwal Inc Due to Fenwal has initiated a...
The Issue: Fenwal has initiated a voluntary Urgent Product Recall for lot FA12C07070 of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-LIFT Inserter Outer Sleeve Product Usage: The Inserter Sleeve is Recalled...
The Issue: The outer sleeve would not fit over the S-LIFT Inserter assembly because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments0400-750-000 T4 Toga Recalled by Stryker Instruments Div....
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-820-000S7 T4 XXL Toga w/T3 Cut Recalled by Stryker...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinook Mini Massager Distributed by www.pinookusa.com. Used to strengthen...
The Issue: Failure to submit a premarket submission and gain approval of a medical device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BC Hammock Mesh Sling (Small) Recalled by Prism Medical Services USA Due to...
The Issue: The product does not meet the firm's size standards, the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BC Hammock Mesh Sling (Large) Recalled by Prism Medical Services USA Due to...
The Issue: The product does not meet the firm's size standards, the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bigliani/Flatow¿ The Complete Solution Fukuda Retractors Small Nonsterile...
The Issue: This is a recall expansion from the 2010 recall which now includes seven...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.