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 47581–47600 of 49,744 recalls
Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...
The Issue: This notice is being provided in follow up to the field correction initiated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posey Biothane Restraint Cuffs Recalled by J T Posey Company Due to The firm...
The Issue: The firm voluntarily recalled Biothane Restraint Cuffs, Catalog No. 2900,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Overhead Rail System Recalled by Hill-Rom, Inc. Due to Liko/Hill-Rom to...
The Issue: Liko/Hill-Rom to date has received two reports from facilities alleging that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical RUMI Arch Recalled by Cooper Surgical, Inc. Due to Excessive...
The Issue: Excessive pressure exerted on the uterine tip when attached to the Arch may,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical Advincula Arch Recalled by Cooper Surgical, Inc. Due to...
The Issue: Excessive pressure exerted on the uterine tip when attached to the Arch may,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraosseous Fixation System (IFS) 1.7 mm Recalled by Orthohelix Surgical...
The Issue: The firm was notified by a customer that there was a burr on the inside end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Digital Diagnost Stationary radiographic system Recalled by Philips...
The Issue: When the operator for a wall stand view selects an "image rotation"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Digital Diagnost Software Version R2.0.2 Product Usage: This system...
The Issue: With Digital Diagnost R2.0.2 a mirrored "R in a circle" is burnt into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Alara Pharmaceutical Co Due to...
The Issue: Subpotent; 15 month stability
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cordis Recalled by Cordis Corporation Due to Affected lots of Cordis ExoSeal...
The Issue: Affected lots of Cordis ExoSeal (TM) VCD have been sterilized using a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiples Anspach Micro Curved Attachments (MCA) and Curved Burr Support...
The Issue: During a recent review of documentation Anspach determined that the current...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter AU5800 Clinical Chemistry Analyzer Recalled by Beckman...
The Issue: Beckman Coulter is recalling the AU8500 Clinical Chemistry Analyzer because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Single Channel Infusion Pumps with Plug-and-Play Modules that...
The Issue: The volume control knob on some Plum A+ single channel infusers (located on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Hyperbaric Single Channel Infusion Pumps with Hospira MedNet...
The Issue: The volume control knob on some Plum A+ single channel infusers (located on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Single Channel Infusion Pumps with Hospira Mednet Software Recalled...
The Issue: The volume control knob on some Plum A+ single channel infusers (located on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiOM Rechargeable Li Ion 22.2 V Battery and BiOM Lithium Recalled by iwalk...
The Issue: Battery may over-heat during charging and smoke
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epinephrine Injection USP Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulates; may contain glass particles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Frozen Yellowfin Tuna Loin 3/5 Recalled by Red Chamber Company Due to Red...
The Issue: Red Chamber is recalling Frozen Yellowfin Tuna Loin due to customer...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips DigitalDiagnost X-Ray System with Eleva Software 2.1.3 Model numbers...
The Issue: When the operator for a wall stand view selects an "image rotation"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Wire Bolt Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Two complaints have been filed where Hoffman LRF Wires have broken during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.