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. 1,820 recalls have been distributed to Delaware in the last 12 months.
Showing 23281–23300 of 48,330 recalls
Recalled Item: Endoform Dermal Template 2x2 Recalled by AROA BIOSURGERY Due to Potential...
The Issue: Potential for pouch seal failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoform Dermal Template 2x2 Recalled by AROA BIOSURGERY Due to Potential...
The Issue: Potential for pouch seal failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoform Dermal Template 4x5 Recalled by AROA BIOSURGERY Due to Potential...
The Issue: Potential for pouch seal failure
Recommended Action: Stop using. Contact the manufacturer or your 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 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: 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: 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: 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: 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: 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: fas.TRACT Coagulative Hemostatic Gel 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.
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: Jay Robb Unflavored Egg White Protein Recalled by Agropur MSI Ingredients...
The Issue: JayRobb Unflavored Egg White Protein Product is being recalled due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
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: 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: 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.