Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,403 recalls have been distributed to Delaware in the last 12 months.
Showing 481–500 of 48,330 recalls
Recalled Item: Allura Xper FD20/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TS-10/TS-10H Tube Sorter Recalled by Sysmex America, Inc. Due to Under...
The Issue: Under specific conditions, the lift's electromagnetic holding force may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is...
The Issue: Potential for defect for Asserachrom HPIA lot 271288, which can affect every...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Plum Duo Infusion Pump Recalled by ICU Medical, Inc. Due to Plum...
The Issue: Plum Solo and Duo Infusion pumps include a feature, that when selected,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glycopyrrolate Oral Solution Recalled by NOVADOZ PHARMACEUTICALS LLC Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ICU Medical Plum Solo Precision IV Pump Recalled by ICU Medical, Inc. Due to...
The Issue: Plum Solo and Duo Infusion pumps include a feature, that when selected,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tom Bumble Nutty Peanut Butter Flake Candy with Peanut & Recalled by Tom...
The Issue: Foreign material.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips Azurion system Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: Philips has identified two (2) software issues affecting device systems that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conductivity Standard Solution Catalog/Model Numbers: 10001 Recalled by...
The Issue: due to a defect associated with the conductivity values of the solution used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) BREAST-HERNIA-PORT...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: CIRCUMCISION PACK...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) PACER / Recalled...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) MEM MAXILLOFACIAL...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) MIDDLE EAR CDS...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment...
The Issue: Due to an error when defining a new stereotactic that users fail to first...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) SMJ LAP Recalled...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment...
The Issue: Due to an error when defining a new stereotactic that users fail to first...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: NERVE BLOCK TRAY 2...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.