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. 2,694 recalls have been distributed to Delaware in the last 12 months.
Showing 2581–2600 of 48,330 recalls
Recalled Item: LOWER EXTREMITY Recalled by American Contract Systems, Inc. Due to Test...
The Issue: Test results for cast padding component included in procedure trays shows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN...
The Issue: Due to a manufacturing defect IV catheter may have a hole in the septum,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timolol Maleate Ophthalmic Solution USP Recalled by FDC Limited Due to...
The Issue: Defective Container: Unable to get the solution out of the bottle as the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: niCARdipine Hydrochloride Injection Recalled by American Regent, Inc. Due to...
The Issue: Lack of sterility assurance: Product leakage around the vial neck, which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: niCARdipine Hydrochloride Injection Recalled by American Regent, Inc. Due to...
The Issue: Lack of sterility assurance: Product leakage around the vial neck, which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Hydrochloride Capsules Recalled by Preferred Pharmaceuticals,...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ropivacaine Hydrochloride Injection Recalled by Amneal Pharmaceuticals, LLC...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bard¿ Single Intragastric Linton Balloon Tube Recalled by C.R. Bard Inc Due...
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check=Flo Performer Introducer Recalled by Cook Incorporated Due to Cook...
The Issue: Cook Medical identified that devices from the affected device lots may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check=Flo Performer Introducer Recalled by Cook Incorporated Due to Cook...
The Issue: Cook Medical identified that devices from the affected device lots may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate) Recalled by C.R....
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) Recalled by C.R. Bard...
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Minnesota Four Lumen Esophagogastric Tamponade Tube Recalled by C.R....
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Blakemore Esophageal-Nasogastric Tube (Adult) Recalled by C.R. Bard Inc...
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments....
The Issue: Incorrect blister labelling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test Recalled by...
The Issue: It was determined that the consumable issue may result in No Call - INT CTL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus Pro Patient Monitor Recalled by Remote Diagnostic Technologies Ltd....
The Issue: software issue that causes an error screen on a portable vital signs monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bone & Joint Restore. 180 capsules in a plastic bottle. Recalled by Optimal...
The Issue: Potential for contamination with salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Urodel Recalled by Pharmadel, LLC Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DoloDent Maximum Strength Toothache Drops Recalled by Pharmadel, LLC Due to...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.