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. 997 recalls have been distributed to Delaware in the last 12 months.
Showing 18501–18520 of 48,330 recalls
Recalled Item: Sterile Cannabidiol (CBD) 50mg/mL Recalled by BIOTA Biosciences LLC Due to...
The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Curcumin Recalled by BIOTA Biosciences LLC Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Curcumin 50mg/mL Recalled by BIOTA Biosciences LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbamazepine Tablets Recalled by Torrent Pharma Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Cannabidiol (CBD) 4mg/mL Recalled by BIOTA Biosciences LLC Due to...
The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Cannabidiol (CBD) + Curcumin 50mg/mL Recalled by BIOTA Biosciences...
The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LACTATED RINGER'S Injection Recalled by ICU Medical Inc Due to Presence of...
The Issue: Presence of Particulate Matter: confirmed customer complaint for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arrow FlexTip Plus Epidural Kit with NRFit Connector Recalled by Arrow...
The Issue: Nine complaints reported that the rotatable collar on the filter had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Healthcare Merge Application Server Software Release and Merge...
The Issue: An error in the calculation of the Michigan Ranges can generate an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The OEC 9900 C-Arm is designed to provide fluoroscopic and Recalled by Ge...
The Issue: GEHC Surgery became aware that some users of the 9800 and 9900 fluoroscopic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker End Cap T2 Tibia +10 mm Catalog Number: 18220010S Recalled by...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker End Cap Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker End Cap T2 Humerus ¿6mm Recalled by Stryker GmbH Due to Seal...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 1 End Cap T2 Humerus ¿6mm Recalled by Stryker GmbH Due to Seal...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Compression Screw Recalled by Stryker GmbH Due to Seal integrity of...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.