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. 2,630 recalls have been distributed to Delaware in the last 12 months.
Showing 11861–11880 of 27,373 recalls
Recalled Item: MoXy Laser Fiber Recalled by Boston Scientific Corporation Due to To...
The Issue: To reinforce existing instructions within the Directions for Use (DFU) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leksell Vantage Stereotactic System. Instrument Carrier Recalled by Elekta...
The Issue: A faulty locking piece of the Instrument Carrier that does not fulfil the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Positron Emission Tomography and Computed Tomography System Recalled by...
The Issue: In affected software version, of Positron emission tomography and computed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERTEX SELECT MULTI AXIAL SCREW. 4.0 X 38MM MULTI AXIAL SCREW. Lot H5517628...
The Issue: Nonconforming product; length of the product measured shorter than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Honey Hydrogel 2"x2" Saturated Gauze- A hydrating wound dressing...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Honey Hydrogel 4"x8" Saturated Gauze- A hydrating wound dressing...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Honey Hydrogel Hydrogel 4oz. Tube. Wound dressing containing...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Honey Hydrogel 4"x4" Saturated Gauze- A hydrating wound dressing...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xience Sierra TM Everolimus Eluting Coronary Stent System Recalled by Abbott...
The Issue: Incorrect expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD-Solis VIP ambulatory infusion pump Recalled by Smiths Medical ASD Inc....
The Issue: Specific Pumps may exhibit intermittent performance in the AILD (Air in Line...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/...
The Issue: The hemostasis valve of aspiration guide catheter devices may fail to seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is Recalled...
The Issue: It was identified that there is a potential for the Stim Interconnecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rapid2 PSU Stim Interconnecting Cable - Product Usage: indicated for...
The Issue: It was identified that there is a potential for the Stim Interconnecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Pleuravideoscope Recalled by Olympus Corporation of the Americas Due...
The Issue: There was no data to validate that the identified endo-therapy devices were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Pleuravideoscope Recalled by Olympus Corporation of the Americas Due...
The Issue: There was no data to validate that the identified endo-therapy devices were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre 5F Plus Over the Wire Embolectomy Catheter Recalled by LeMaitre...
The Issue: There has been an increased trend in reports of catheters failing to deflate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Utak NR Trace Elements Serum Control Recalled by Utak Laboratories Inc Due...
The Issue: The product has an incorrect value for cadmium and an incorrect expected range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifePAK 500 Automated External Defibrillator Recalled by Physio-Control,...
The Issue: Automated External Defibrillators may not detect a patient connection due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X12+ and patient cable for the X12+ Telemeter with the Recalled by WELCH...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lead diagnostic electrocardiograph under the following device names: ELI 10...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.