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. 2,489 recalls have been distributed to Mississippi in the last 12 months.
Showing 20981–21000 of 49,744 recalls
Recalled Item: Mometasone Furoate Cream USP Recalled by Glenmark Pharmaceuticals Inc., USA...
The Issue: GMP Deviations: Glenmark received complaints stating that mometasone fuorate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 'n'-Hole Post which is a component of the Revolution External Recalled by...
The Issue: The threads on posts stripping out when tensioned during application process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammomat Revelation with software version VC10 and Biopsy Option Intended...
The Issue: An error can occur when performing a biopsy using the InSpect function. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190...
The Issue: Inaccurately Low Sample Results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Online TDM Vancomycin Gen.3 ( 200 tests) Catalog # 06779344190 Recalled by...
The Issue: Inaccurately Low Sample Results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...
The Issue: Acetabular liners failed the oxidation testing performed prior to release....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...
The Issue: Acetabular liners failed the oxidation testing performed prior to release....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...
The Issue: Acetabular liners failed the oxidation testing performed prior to release....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Folate 100 test kit-for IVD of folate Recalled by...
The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Folate (500 Test Kit)-for IVD of folate Recalled by...
The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Folate (500 Test Kit )- for IVD Recalled by Siemens...
The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynex DSX Software-IVD ELISA Assays effected as follows: DSX Assay Recalled...
The Issue: Assay files used on the open Dynex DSX Instrument to process IVD ELISA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge MCC Flow i Disposable CO2 absorber Recalled by GETINGE US SALES LLC...
The Issue: Reversed expiration and manufacturing date on the label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Enteral Safe Feeding Tubes: a) Recalled by DeRoyal Industries Inc...
The Issue: Certain MED-RX Polyurethane Feeding Tubes are being recalled due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisinopril and Hydrochlorothiazide Tablets USP Recalled by Lupin...
The Issue: Presence of Foreign Tablets/Capsules: Product complaint received of one...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MONSEL'S (Ferric Subsulfate) Solution Recalled by Dercher Enterprises, Inc.,...
The Issue: Microbial Contamination of Non-Sterile Products and Superpotent Drug: FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NobelActive Internal NP 3.5x15mm Endosseus dental implant Recalled by Nobel...
The Issue: The top label for dental implant may incorrectly indicate the implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips 5-Lead Set Recalled by Philips North America, LLC Due to The...
The Issue: The thickness of the connector to the trunk cable on affected limb lead sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm FDR Go Plus mobile X-ray system Recalled by Fujifilm Medical...
The Issue: The graphics driver of the FDR Go PLUS might cause the appearance of a Blue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-TEMP LT System Recalled by Cincinnati Sub-Zero Products LLC, a...
The Issue: Updated Manual-Warnigs have been added stating that exceeding 40'C for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.