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. 2,577 recalls have been distributed to Delaware in the last 12 months.
Showing 15841–15860 of 27,373 recalls
Recalled Item: ST AIA-PACK¿ PROG III Recalled by Tosoh Bioscience Inc Due to Falsely...
The Issue: Falsely elevated progesterone assay values will occur when using certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x100mm 5.0ml PLBL Gold...
The Issue: Tubes may exhibit stopper creepout/pullout, where the stopper dissociates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RaPET¿ RF Latex Reagent used as a component in the Recalled by Stanbio...
The Issue: All patient serum samples yield a weakly positive test result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK¿ PROG II Recalled by Tosoh Bioscience Inc Due to Falsely...
The Issue: Falsely elevated progesterone assay values will occur when using certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x75mm 3.5ml PLBL Gold...
The Issue: Tubes may exhibit stopper creepout/pullout, where the stopper dissociates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Video Duodenoscope Model: ED-3490TK (UDI of design being recalled:...
The Issue: The duodenoscopes are being recalled in order to replace the forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quick Connect 272 KG Scale used with Maxi Sky 2 Recalled by Arjohuntleigh...
The Issue: The spreader bar can detach from the scale attachment under certain conditions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q-Connect 272 KG Scale used with Maxi Sky 2 ceiling Recalled by...
The Issue: The spreader bar can detach from the scale attachment under certain conditions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stanbio AC power adapter for the HemoPoint H2 meter Recalled by Stanbio...
The Issue: The US prong (type A) adapter plate may crack, break, or detach and remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore (Oncology) - Model no. 728243 Recalled by Philips...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE isp Implantable Port With Smooth Septum and Attachable...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT(R) ClearVUE(R) isp with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore (Radiology) - Model no. 728244 Recalled by Philips...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.