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. 997 recalls have been distributed to Delaware in the last 12 months.
Showing 20881–20900 of 48,330 recalls
Recalled Item: Gold Cup Leadwire and Snap Leadwire with the following component Recalled by...
The Issue: The electrode lead connector has a protruding conductor beyond insulation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightPod Neo Lasers Recalled by Aerolase Corporation Due to This relates to...
The Issue: This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightPod ERA lasers Recalled by Aerolase Corporation Due to This relates to...
The Issue: This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Recalled...
The Issue: Possible presence of small plastic pieces caused by a manufacturing failure.
Recommended Action: Do not consume. Return to store for a refund or discard.
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.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.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: 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: 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.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: 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: 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.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: 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.
Recalled Item: Sheridan/HVT Novaplus: a) 7.0 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: 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: 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: 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: Sheridan/CF Novaplus 7.0 mm Recalled by Teleflex Medical Due to Reported...
The Issue: Reported complaints indicate an increased incidence of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.