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. 2,649 recalls have been distributed to Delaware in the last 12 months.
Showing 9221–9240 of 13,379 recalls
Recalled Item: Stree Overlord Recalled by R Thomas Marketing, LLC Due to Marketed Without...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Black Ant Recalled by R Thomas Marketing, LLC Due to Marketed Without An...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Weekend Prince Recalled by R Thomas Marketing, LLC Due to Marketed Without...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Real Skill Recalled by R Thomas Marketing, LLC Due to Marketed Without An...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Guaifenesin DM Cherry liquid (guaifenesin 100 mg/5 mL and Dextromethorphan...
The Issue: Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Guaifenesin Grape liquid 100 mg/5 mL Recalled by Perrigo Company PLC Due to...
The Issue: Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magnesium Sulfate in Water for Injection Recalled by Hospira Inc. Due to...
The Issue: Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Mayne Pharma Usa Due to Lack...
The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate Recalled by Pharmedium Services, LLC Due to...
The Issue: Subpotent Drug; confirmed results by FDA analysis after customer complaints...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Sandoz Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications; 9 month stability timepoint
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate Recalled by Pharmedium Services, LLC Due to...
The Issue: Subpotent Drug; confirmed results by FDA analysis after customer complaints...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets 0.125 mg Recalled by Macleods Pharma Usa...
The Issue: Presence of Foreign Tablets/Capsules: Presence of a comingled Carbimazole 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: APEXXX tablets Recalled by Nuway Distributors, LLC Due to Marketed Without...
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Capecitabine tablets USP 500 mg Recalled by Teva North America Due to Failed...
The Issue: Failed Dissolution Specifications: low test results at the 18 month time-point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.