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 25981–26000 of 28,172 recalls
Recalled Item: DMLC IV-ERGO Product Usage: Intended for use with rotating gantry Recalled...
The Issue: It is possible for an intermittent error to occur in the gantry sensor of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar 360. Designed to meet the needs for lifting humans. Recalled by...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics Micro Introducer Kits under the following labeling: 1)...
The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity 3.0 Product Usage: The Agility multileaf collimator is indicated...
The Issue: Unexpected movement during beam delivery may not be detected if there are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: adult defibrillation Recalled by TZ Medical Inc. Due to TZ Medical Inc is...
The Issue: TZ Medical Inc is recalling its P-211-M1 and P-214-M1 Medtronic / Physio...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar Wide 670. Designed to meet the needs for lifting humans. Recalled...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ Breathe Atomizer Model # EZ-100. For the delivery of Recalled by Nephron...
The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AsthmaNefrin Starter Kit contains ten (10) AsthmaNefrin vials and one...
The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TX1 Tissue Removal System disposable handpieces. Product Usage: The TX1...
The Issue: American Optisurgical, Inc. is recalling certain lots of TX1 Tissue Removal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar 350. Designed to meet the needs for lifting humans. Recalled by...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar Standard. Designed to meet the needs for lifting humans. Recalled...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics VenaCure EVLT NeverTouch-FRS PROCEDURE KIT under the following...
The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FAST Procedure Kit. Intended for use as a Minor Surgical Procedures Tray....
The Issue: American Optisurgical, Inc initiated a recall of ChloraPrep Hi-Lite Orange...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ Breathe Medication Cup. For the delivery of liquid medications Recalled...
The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Trauma Phoenix Retrograde Femoral Connecting Bolt Trauma Fixation...
The Issue: Biomet Trauma ("Biomet") has initiated a recall of Retrograde Femoral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardio Medical Products Recalled by Cardio Medical Products Due to Covidien...
The Issue: Covidien received customer reports of Arcing/Sparking on the defibrillation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU2700 Clinical Chemistry Analyzer AU5400 Clinical Chemistry Analyzer...
The Issue: Beckman Coulter is recalling AU2700/AU2700 Plus & AU5400 Clinical Chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B-CrossLaps/serum (B-CTx in serum) 160 100 tests Immunoassay Recalled by...
The Issue: Roche Diagnostics internal investigations in R&D have shown that the claims...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******iMRI Handpiece. Use with iMRI System Only***Rx Only***Manufacturer:...
The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluoroscan Mini C-arm InSight Recalled by Hologic, Inc. Due to The audible...
The Issue: The audible alarm to alert the operator when cumulative irradiation time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.