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. 2,489 recalls have been distributed to Mississippi in the last 12 months.
Showing 21301–21320 of 28,172 recalls
Recalled Item: Taut Intraducers 10/BX7.5 FR 3.5 Recalled by Teleflex Medical Due to The...
The Issue: The defective component can cause gas leakage through the device. This can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune Plus Recalled by TZ Medical Inc. Due to The IFU of the Neptune Plus...
The Issue: The IFU of the Neptune Plus Pads, does not match that submitted in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspiration Ventilator System Recalled by Event Medical LTD Due to A...
The Issue: A component on the systems power board can fail in a manner which can cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovoCut Suture Manager Recalled by Ceterix Orthopedics, Inc. Due to The...
The Issue: The NovoCut Suture Manager device may cut the suture during knot tensioning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Two-stage and three-stage I.V. poles are shipped as an optional Recalled by...
The Issue: It was identified by a customer complaint that some I.V. poles were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access CEA Assay Recalled by Beckman Coulter Inc. Due to Beckman Coulter is...
The Issue: Beckman Coulter is recalling the Access CEA reagent packs because they were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartSite Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion...
The Issue: CareFusion is recalling the SmartSite Extension Set due to disconnection and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: miraDry System consisting of the MD4000-MC Console Recalled by Miramar Labs,...
The Issue: Update to labeling for the miraDry Console to remind users to only use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Notch Titanium Reconstructive Plate set (SNTRP). Ti...
The Issue: The Synthes SNTRP set was released for sale as a Trauma product in 1996 with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shuttle Select Slip-Cath Catheter. Angiographic catheter. For use in...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom 100 Low Bed (GPAC) AC Powered adjustable hospital bed Recalled by...
The Issue: Hill-Rom is voluntarily recalling the Hill-Rom 100 Low Bed due to complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Threaded Plate Holder- Long for 3.5mm Locking Hold Recalled by...
The Issue: The affected part number and lot listed above is incorrectly etched with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helioseal F Sealant 1 x 1.25 g Recalled by Ivoclar A. G. Due to A defect...
The Issue: A defect occurred in the production process of Helioseal F Sealant; the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry XPT Systems Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Multiple Software issues. Auto Start-UP Fail, Calibration Interval Resets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Antibacterial Hydro Personal Catheter Recalled by C.R. Bard, Inc. Due to...
The Issue: Incorrect unit labeling. The case label and shelf box are correct, Product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn KleenSpec Corded Illumination System Recalled by Welch Allyn Inc...
The Issue: The firm became aware that the KleenSpec¿ 788 Corded Illuminator has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triton Infusion Pump (model 300000) and Triton fp Infusion Pump Recalled by...
The Issue: The device might fail to detect air in line while infusing the medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips X-Ray Systems Recalled by Philips Electronics North America...
The Issue: Upon initiating Fluoroscopy the user may encounter a user message Fluoro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The "Pacifier Activated Lullaby" (PAL) System composed of three major...
The Issue: PAL unit has undergone significant technological changes since the previous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. Merge Cardio is a system intended to Recalled by...
The Issue: Reporting feature times out after inactivity for more than an hour sending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.