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. 2,457 recalls have been distributed to Delaware in the last 12 months.
Showing 26701–26720 of 27,373 recalls
Recalled Item: Edwards Lifesciences Rigid Suction Wand Recalled by Edwards Lifesciences,...
The Issue: Edwards is recalling Suction Wand models SPC2081 and S033 because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL80 FLEX (with FLEX software) and ABL80 FLEX CO-OX (with Recalled by Sendx...
The Issue: The firm recalled because the glucose measurements from a patient sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Ultraview DM3 Monitor Model Number: 91330-NT The Ultraview DM3...
The Issue: Unit fails to power up, resulting in an equipment alarm
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo.plaza radiological image processing system. Recalled by...
The Issue: Siemens became aware of an unintended behavior when using syngo.plaza. In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PathFinder NXT Pivoting Percutaneous Rod Holder This device is an Recalled...
The Issue: Complaints have been reported where, during surgery, the surgeon was unable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Button Switchpens Recalled by PSC Industries Inc Due to The Tyvek pouch...
The Issue: The Tyvek pouch label for this device states: 'with holster'; however, this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pathfinder NXT Fixed Percutaneous Rod Holder Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer is recalling Pathfinder NXT Fixed Percutaneous Rod Holder, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pathfinder NXT Fixed Percutaneous Rod Holder Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer is recalling Pathfinder NXT Fixed Percutaneous Rod Holder, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Button Switchpens Recalled by PSC Industries Inc Due to The carton label for...
The Issue: The carton label for this device has the manufacturer symbol where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica M525 F50 Surgical Microscope Recalled by Leica Microsystems, Inc. Due...
The Issue: Leica Microsystems evaluated data showing that a malfunction resulting in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap(R) - Miethke Shunt System Recalled by Aesculap, Inc. Due to The...
The Issue: The deflector may not move freely on the ventricular catheter. The deflector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...
The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XE-2100C Automated Hematology System Recalled by Sysmex America, Inc....
The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XE-2100 Automated Hematology System Recalled by Sysmex America, Inc....
The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...
The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XE-5000 Automated Hematology System Recalled by Sysmex America, Inc....
The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Insulated Tips Recalled by PSC...
The Issue: Firm officials reported to CIN-DO that the outer carton label of this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 8.25 (209.6 mm) 0.5mm Tips Recalled by PSC Industries Inc...
The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Non-Insulated Tips Recalled by PSC...
The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 8.5" (215.9mm) Serrated 1.0 mm Tips...
The Issue: Firm officials reported to CIN-DO that their Electrosurgical Monopolar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.