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. 2,590 recalls have been distributed to Mississippi in the last 12 months.
Showing 14601–14620 of 28,172 recalls
Recalled Item: IMRIS ORT 200 Recalled by Deerfield Imaging, Inc. Due to Table may drift in...
The Issue: Table may drift in the roll position while in use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8Fr SAFE GRAD CAT W/Valve (Argyle Suction Catheter Kits with Chimney Valve)...
The Issue: The product was released into commercial distribution while subject to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F160NR Capillary High Flux Dialyzer Single Use Only Recalled by...
The Issue: Potential for external blood leaks from the dialyzer header
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated...
The Issue: Cosmetic imperfections on the surface of some lenses.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 700 Thyroid Uptake System Recalled by Capintec Inc Due to There is a...
The Issue: There is a potential for the spring arm failure as a result of a broken...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 3000 Thyroid Uptake System Recalled by Capintec Inc Due to There is a...
The Issue: There is a potential for the spring arm failure as a result of a broken...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Coupler Forceps Recalled by Baxter Healthcare Corporation Due to...
The Issue: Potential presence of rust on Coupler Forceps (GEM4183C).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEPHANIX D2RS Digital Dynamic Remote...
The Issue: The firm has detected a potential risk using the command. After releasing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ascom Telligence Nurse Call System Recalled by Ascom (US) Inc. Due to There...
The Issue: There is an issue that could cause the Telligence System Gateway II, NGGTWY2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadPRO(R) Mobile 40kW Digital X-Ray System - Model: SM-40HF-B-D-C Product...
The Issue: There is a potential for the RadPRO Mobile 40kW Digital X-Ray System Model...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN Heater-Cooler System 3T 120V~/60Hz Description of product: Recalled by...
The Issue: The firm has become aware that due to a chemical reaction, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS NT-proBNP Reagent Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to The...
The Issue: The firm is extending their previous July 2018 recall to include additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Anti-HBe Reagent Pack Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to...
The Issue: The firm is extending their previous July 2018 recall to include additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantikine¿ IVD¿ ELISA Recalled by R & D Systems, Inc. Due to The Human sTfR...
The Issue: The Human sTfR Quantikine IVD ELISA Kit, catalog # DTFR1, lot P180151 was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS HBeAg Reagent Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to The firm...
The Issue: The firm is extending their previous July 2018 recall to include additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The SQ-RX Pulse Generator a component of the Subcutaneous Implantable...
The Issue: Experienced accelerated battery depletion and a shortened replacement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne CDx Test Results Recalled by Foundation Medicine, Inc. Due to...
The Issue: An incorrect test result for a single analyte may have been reported for up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.