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 2421–2440 of 13,379 recalls
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...
The Issue: Defective Container: Complaints received of vial breakage and glass flying...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Desmopressin Acetate Tablets 0.2mg Recalled by Heritage Pharmaceuticals Inc...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sensorcaine (Bupivacaine HCl and Epinephrine Injection Recalled by Fresenius...
The Issue: Subpotent Drug: Testing results below the defined limit for the epinephrine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sensorcaine-MPF (Bupivacaine HCl and Epinephrine Injection Recalled by...
The Issue: Subpotent Drug: Testing results below the defined limit for the epinephrine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sensorcaine (Bupivacaine HCl and Epinephrine Injection Recalled by Fresenius...
The Issue: Subpotent Drug: Testing results below the defined limit for the epinephrine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Fresenius Medical Care Holdings,...
The Issue: Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allergy Relief D Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: Recalled lot was found to be out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Sulfacetamide 10% Sulfur 4% Cleansing Pads Recalled by Acella...
The Issue: Subpotent drug: Out of specification for assay at the end-of-shelf-life...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenytoin Sodium Injection Recalled by Acella Pharmaceuticals, LLC Due to...
The Issue: Labeling: Not elsewhere classified; the product is being recalled because of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenytoin Sodium Injection Recalled by Acella Pharmaceuticals, LLC Due to...
The Issue: Labeling: Not elsewhere classified; the product is being recalled because of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenoxybenzamine Hydrochloride Capsules Recalled by Par Formulations Private...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-Neostigmine Methylsulfate Injection Recalled by Nephron Sterile...
The Issue: CGMP Deviations: Potential for cross contamination due to product carry over.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-Labetalol HCl Injection Recalled by Nephron Sterile Compounding Center...
The Issue: CGMP Deviations: Potential for cross contamination due to product carry over.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamterene and Hydrochlorothiazide Capsules Recalled by Lannett Company...
The Issue: Failed Impurity/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamterene and Hydrochlorothiazide Capsules Recalled by Lannett Company...
The Issue: Failed Impurity/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol-Latanoprost (0.5/0.005%) ophthalmic drops Recalled by ImprimisRx NJ...
The Issue: Subpotent Drug: The batches contain less than 90% of the labeled amount of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...
The Issue: Lack of assurance of sterility: Bags have the potential to leak in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adam's Polishes ALCOHOL BASED HAND SANITIZER Recalled by Adam's Polishes LLC...
The Issue: CGMP Deviations: Other lots of hand sanitizer are being recalled because...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adam's Polishes ALCOHOL BASED HAND SANITIZER Recalled by Adam's Polishes LLC...
The Issue: Chemical Contamination: FDA analysis found 1 lot of Adam's Polishes ALCOHOL...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.