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. 1,050 recalls have been distributed to Delaware in the last 12 months.
Showing 11321–11340 of 27,373 recalls
Recalled Item: Orthopedics 6.0MM ROD Recalled by OrthoPediatrics Corp Due to Product may...
The Issue: Product may have incorrect laser etched alignment lines, the non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 004551004 GTIN: 24026704553796 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 0004550003 GTIN: 14026704663078 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 (each) - Product...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 004551003 GTIN: 14026704663122 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 004551002 GTIN: 14026704663115 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 004550004 GTIN: 14026704663085 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex PS-10 Sample Preparation System Catalog number:BQ716341 - Product...
The Issue: Insufficient amount of antibody without an error message or alarm
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DYNEX Agility Recalled by Dynex Technologies, Inc. Due to Control samples...
The Issue: Control samples aspirated from wrong SmartKit on the Agility. Agility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6' (15 cm) Appx 0.09 ml Recalled by ICU Medical, Inc. Due to Incorrect...
The Issue: Incorrect filter assemblies in IV administration set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Module Model 8110 - Product Usage: is intended Recalled by...
The Issue: LED display, which provides infusion or patient monitoring values, on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearPro T-Piece Closed Suction Catheter Recalled by Medline Industries Inc...
The Issue: There are reports of the suction catheter coming apart from the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pleur-Evac Adult-Ped Wet Recalled by TELEFLEX MEDICAL INC Due to Potential...
The Issue: Potential for sterile packaging to be compromised¿
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressa Bed Recalled by Hill-Rom, Inc. Due to Affected beds may have...
The Issue: Affected beds may have screws installed that do not meet material tensile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Module Model 8110 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC Unit Model 8000 modular infusion pump and monitoring system...
The Issue: If one or more screws or washers are loose or missing causing the battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Model 8100 - Product Usage: is intended Recalled by...
The Issue: LED display, which provides infusion or patient monitoring values, on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris SpO2 Module Model 8210 and Model 8220 - Product Recalled by...
The Issue: LED display, which provides infusion or patient monitoring values, on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PCA Module Model 8120 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC Unit Model 8000 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.