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 19941–19960 of 48,330 recalls
Recalled Item: UP2 Recalled by Med Man Distribution, Inc. Due to Undeclared Sildenafil
The Issue: Marketed without an Approved NDA/ANDA: Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cognision Recalled by Neuronetrix Solutions, LLC dba Cognision Due to...
The Issue: Product has the potential to be contaminated with Burkholderia cepacia (B....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ligamax 5 mm Endoscopic Multiple Clip Applier Recalled by Ethicon...
The Issue: A potential exists that certain LIGAMAX devices within the impacted lots may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iChem VELOCITY Urine Chemistry Analyzer Recalled by Beckman Coulter Inc. Due...
The Issue: Beckman Coulter has become aware of an issue affecting Specific Gravity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freshness Guaranteed Croissants in clear plastic 12oz clamshell Recalled by...
The Issue: Product is missing ingredient and nutrition label on bottom of clamshell...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The FastPack System Comlete Immunoassay Kit Immunoassay for the Quantitative...
The Issue: The chemiluminescent immunoassay has been noted to have higher than expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Color Cuff Disposable Tourniquet Cuff Recalled by Stryker Instruments Div....
The Issue: There is a potential for the cuff to leak air leading to a loss of vascular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Color Cuff Disposable Tourniquet Cuff Recalled by Stryker Instruments Div....
The Issue: There is a potential for the cuff to leak air leading to a loss of vascular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aurobindo Ranitidine Capsules 300 mg Recalled by AuroMedics Pharma LLC Due...
The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DG Health Acid Reducer Ranitidine Tablets 150 mg Recalled by AuroMedics...
The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aurobindo Ranitidine Caspules 150 mg Recalled by AuroMedics Pharma LLC Due...
The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution Recalled by AuroMedics Pharma LLC...
The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aurobindo Ranitidine Capsules 150 mg Recalled by AuroMedics Pharma LLC Due...
The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...
The Issue: The products may have been packaged with an incorrect Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...
The Issue: The products may have been packaged with an incorrect Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...
The Issue: The products may have been packaged with an incorrect Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...
The Issue: The products may have been packaged with an incorrect Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...
The Issue: The products may have been packaged with an incorrect Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dako Autostainer instruments: Autostainer Link 48 Recalled by Dako Denmark...
The Issue: The Autostainer instrument may not have a syringe tray installed which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haylard Closed Suction System for Neonates/Pediatrics Recalled by Avanos...
The Issue: Avanos Medical has received reports stating that the central lumen of some 5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.