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. 2,448 recalls have been distributed to Mississippi in the last 12 months.
Showing 31181–31200 of 49,744 recalls
Recalled Item: Brilliance 64 728231 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...
The Issue: An increase in reports indicating that the reprocessed H12LP Trocar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...
The Issue: Lack of 510k clearance for design modification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...
The Issue: Lack of 510k clearance for design modification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Light Body Fast Set Wash Material Recalled by Ivoclar Vivadent,...
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAM Kirschner Wire Recalled by Stryker Howmedica Osteonics Corp. Due to A...
The Issue: A review of packaging revealed the seal integrity of the pouch may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard C-Section Drape with Clear Screen and Full Incise (Non-Sterile)...
The Issue: Drapes within the affected lots may include a manufacturing variation that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Test Pack Heavy/Light Fast Set Recalled by Ivoclar Vivadent, Inc....
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4.0 Recalled by RAYSEARCH LABORATORIES AB Due to Software...
The Issue: Software anomaly; an issue was found with the proton Pencil Beam Scanning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Light Body Regular Set Wash Material Recalled by Ivoclar...
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Free2b Sun Cups Chocolate. Made With SunButter Sunflower Spread. Packaged...
The Issue: Free2b Foods recalled the Sun Cups Chocolate due to potential contamination...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: L-Cysteine Hydrochloride Injection Recalled by Sandoz Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: bulk solution tested...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: L-Cysteine Hydrochloride Injection Recalled by Sandoz Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Techni-Care Surgical Hand Scrub and Patient Preoperative Skin Preparation...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date - Product is missing or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CANNIBAL FEROX AMPED Recalled by Chaos and Pain Due to Product was analyzed...
The Issue: Product was analyzed and found to contain 1,3- dimethylbutylamine which was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Performance-LOAD Ambulance Cot Fastener Stretcher Recalled by Stryker...
The Issue: Stryker Medical initiated a voluntary recall of Stryker Performance-LOAD Cot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Ported Aspiration System Tray Recalled by Teleflex Medical...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Bone Lesion Biopsy System Tray Recalled by Teleflex Medical...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Bone Marrow Biopsy System Tray Recalled by Teleflex Medical...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.