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. 1,035 recalls have been distributed to Mississippi in the last 12 months.
Showing 20861–20880 of 49,744 recalls
Recalled Item: CAIMAN DISP.INSTR.ARTICULAT.D:12/440MM Product Usage: Instrument intended...
The Issue: possibility of the sterility batch being insufficiently sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superset with 22MM ID Recalled by Intersurgical Inc Due to The port may...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Recalled by...
The Issue: Products may contain the incorrect banner card within the kit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8.5 Fr. X 10 cm ARROW+gard Blue PSI Kit Cath-Gard Recalled by Arrow...
The Issue: Products may contain the incorrect banner card within the kit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuardian Heart Remote Monitoring Kit Recalled by Preventice Services,...
The Issue: The device data being collected and transferred to the monitoring center may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Short Fill: fill...
The Issue: Short Fill: fill volume was out of specification at 94 mL (specification: no...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PreGel Lemon 50 4.4 lb (2kg) bag Recalled by PreGel America, Inc. Due to...
The Issue: Undeclared Milk. The firm received a complaint that there was milk in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Recalled...
The Issue: Possible presence of small plastic pieces caused by a manufacturing failure.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gold Cup Leadwire and Snap Leadwire with the following component Recalled by...
The Issue: The electrode lead connector has a protruding conductor beyond insulation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightPod ERA lasers Recalled by Aerolase Corporation Due to This relates to...
The Issue: This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightPod Neo Lasers Recalled by Aerolase Corporation Due to This relates to...
The Issue: This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rocket KCH Fetal Bladder Drainage Catheter Model: R57405 Recalled by Rocket...
The Issue: A complaint was received regarding kinking of the device prior to use. If a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Now Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Top Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 Nerve Monitor Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Stryker C2 NerveMonitor's design and instructions may not optimally address...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.All Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.