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. 995 recalls have been distributed to Delaware in the last 12 months.
Showing 23281–23300 of 48,330 recalls
Recalled Item: Amlodipine and Valsartan Tablets 10 mg/320 mg (a) 30-count bottles Recalled...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Recalled by Teva Pharmaceuticals USA Due to CGMP Deviations: FDA...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Recalled by Teva Pharmaceuticals USA Due to CGMP Deviations: FDA...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: infants* IBUPROFEN Recalled by Tris Pharma Inc. Due to Superpotent Drug:...
The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...
The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...
The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: da Vinci X Surgical System Recalled by Intuitive Surgical, Inc. Due to Due...
The Issue: Due to a manufacturing variation in the arm that can result in a persistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to Due...
The Issue: Due to a manufacturing variation in the arm that can result in a persistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...
The Issue: The power load floor plates which hold the ambulance cot anchors in place...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrex Suture Anchor Recalled by Arthrex, Inc. Due to Potentially lead to...
The Issue: Potentially lead to anchor breakage during insertion,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HeartWare Ventricular Assist HVAD System Battery Charger Model...
The Issue: HVAD Battery Charger units manufactured with wrong inductors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical Confirm Rx Insertable Cardiac Monitor Recalled by Abbott...
The Issue: The device is unable to pair with the mobile app due to the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyberonics VNS Therapy AspireHC Model 105 Generator Recalled by LivaNova USA...
The Issue: This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyberonics VNS Therapy AspireSR Recalled by LivaNova USA Inc Due to This...
The Issue: This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare 9805 and 9805P Hydraulic Patient Lifts Recalled by Invacare...
The Issue: Invacare has identified via customer complaints, the potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LivaNova VNS Therapy System Recalled by LivaNova USA Inc Due to Lead...
The Issue: Lead impedance values reported by the affected VNS generator will be higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2 Recalled by LivaNova USA...
The Issue: This recall is being initiated due to reports that that the therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BeeGentle Honey Flavored Topical Anesthetic Recalled by CAO Group, Inc. Due...
The Issue: cGMP violations noted during the firm's most recent inspection.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SHEER DesenZ Desensitizing Treatment Recalled by CAO Group, Inc. Due to cGMP...
The Issue: cGMP violations noted during the firm's most recent inspection.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FastStat Topical Hemostat Introductory Kit Recalled by CAO Group, Inc. Due...
The Issue: cGMP violations noted during the firm's most recent inspection.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.