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. 2,635 recalls have been distributed to Mississippi in the last 12 months.
Showing 5521–5540 of 28,172 recalls
Recalled Item: DigitalDiagnost C90 Flex/Value/Chest/ER Recalled by Philips North America...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Flex/Value Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8713051U Recalled by B. Braun Medical, Inc. Due to Upstream occlusion alarm...
The Issue: Upstream occlusion alarm may sound when no occlusion exists, and the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8713052U Recalled by B. Braun Medical, Inc. Due to Upstream occlusion alarm...
The Issue: Upstream occlusion alarm may sound when no occlusion exists, and the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack Recalled by...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 20 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject" 60 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject" 12 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject" 6 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject" 35 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuroSync EYE-SYNC containing Pico Neo 2 Headsets. Each unit consists...
The Issue: Eye syncing issues causing the device to be inoperable. Unable to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeadCare II Blood Lead Test Kit-For in vitro diagnostic use Recalled by...
The Issue: During an internal audit a small percentage (<10%) of plastic caps used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Express Dry Seal Chest Drains (Express): 4000-100N DRAIN Recalled by Atrium...
The Issue: Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ocean Water Seal Chest Drains (Ocean): Products Product Recalled by Atrium...
The Issue: Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oasis Dry Suction Water Seal Chest Drains (Oasis): (1)3600-100 DRAIN...
The Issue: Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBA Proton Therapy System - PROTEUS 235. PTS-11 versions Recalled by Ion...
The Issue: The patient positioning system can perform motions in unexpected directions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Stat Profile Prime Plus POC Analyzer (CE)-Intended to measure Recalled...
The Issue: Potential risk of reporting erroneous creatinine patient results associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Biomedical Prime Plus Analyzer -Intended to measure certain gases in...
The Issue: Potential risk of reporting erroneous creatinine patient results associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PCA Module 8120 Recalled by CareFusion 303, Inc. Due to Alaris PCA...
The Issue: Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.