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. 2,620 recalls have been distributed to Delaware in the last 12 months.
Showing 12921–12940 of 27,373 recalls
Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder...
The Issue: Separation of front and rear barrels upon activation of the safety feature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 Nerve Monitor Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Stryker C2 NerveMonitor's design and instructions may not optimally address...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 Nerve Monitor Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Stryker C2 NerveMonitor's design and instructions may not optimally address...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Top Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Top Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Now Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.All Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.All Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digital Medical X-ray Imaging System Recalled by Shanghai United Imaging...
The Issue: X-ray imaging system positioning image and protocol label is reversed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiForce GX560 monochrome LCD monitor Recalled by Eizo Corporation Due to...
The Issue: Under certain conditions, a marble pattern infrequently appears on the monitor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiForce RX360 Recalled by Eizo Corporation Due to Under certain...
The Issue: Under certain conditions, a marble pattern infrequently appears on the monitor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Atellica CH 930 Analyzer. Siemens Material Number (SMN): 11067000...
The Issue: Atellica CH 930 Analyzer - Erroneous Indices for Hemolysis and Lipemia in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan/CF: a) 3.0 mm Recalled by Teleflex Medical Due to...
The Issue: Reported complaints indicate an increased incidence of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan EZ-ENDO: a) 5.0 mm Recalled by Teleflex Medical Due to...
The Issue: Reported complaints indicate an increased incidence of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan/HVT: a) 5.0 mm Recalled by Teleflex Medical Due to...
The Issue: Reported complaints indicate an increased incidence of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan Preformed: a) 3.0 mm Recalled by Teleflex Medical Due to...
The Issue: Reported complaints indicate an increased incidence of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan Uncuffed: a) 2.0 mm Recalled by Teleflex Medical Due to...
The Issue: Reported complaints indicate an increased incidence of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan LTS: a) 4.0 mm Recalled by Teleflex Medical Due to...
The Issue: Reported complaints indicate an increased incidence of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.