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. 1,069 recalls have been distributed to Delaware in the last 12 months.
Showing 9501–9520 of 27,373 recalls
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse Cardiovascular (Synapse CV). Software Versions: 6.0 to 6.2.1 The...
The Issue: Software versions 6.0.4 to 6.2.1 using Advanced Reporting -possibility that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE Control Set - IVD Control set for the quantitative Recalled by Sentinel...
The Issue: Claim for stability after reconstitution from lyophilized to liquid form...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Myriad-LX Light Source-for delivery of light to the surgical field Recalled...
The Issue: (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NICO Myriad-LX Illumination Pack: Mvriad-LX Illumination Pack. 11ga Recalled...
The Issue: (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY10Z48R2 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic BB9G78R8 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB10R79R6 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB4W67R20 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB1H18R20 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB7J98R7 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY10J00R12 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.