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. 2,695 recalls have been distributed to Delaware in the last 12 months.
Showing 881–900 of 48,330 recalls
Recalled Item: NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP...
The Issue: Tape used to secure components within packaging contains latex, despite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination...
The Issue: Tape used to secure components within packaging contains latex, despite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Premium Kratom Green Maeng Da powder is packaged in Recalled by...
The Issue: Product has the potential to be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Monarch Premium Kratom White Elephant powder is packaged in seal Recalled by...
The Issue: Product has the potential to be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Monarch Premium Kratom Red Bali powder is packaged in seal Recalled by Lotus...
The Issue: Product has the potential to be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Monarch Premium Kratom Bali Gold powder is packaged in seal Recalled by...
The Issue: Product has the potential to be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medicrea Recalled by Medicrea International Due to Due to complaints,...
The Issue: Due to complaints, orthopedic rotation tool handle may untread from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by Otsuka ICU Medical LLC Due to Labeling:...
The Issue: Labeling: Label Error on Declared Strength-The overwrap label may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by Otsuka ICU Medical LLC Due to Labeling:...
The Issue: Labeling: Label Error on Declared Strength-The overwrap label may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medicrea Recalled by Medicrea International Due to Due to complaints,...
The Issue: Due to complaints, orthopedic rotation tool handle may untread from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CT 5300 Recalled by Philips North America Llc Due to If the screws of tube...
The Issue: If the screws of tube heat exchanger on the rotating scanner are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT Recalled by Philips North America Llc Due to If the screws of...
The Issue: If the screws of tube heat exchanger on the rotating scanner are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aurora EV-ICD and Clinical EV-ICD Recalled by Medtronic, Inc. Due to There...
The Issue: There is a potential for delayed time to high-voltage (HV) therapy should a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agebox iKids-Growth (Night Formula) Recalled by Agebox Due to Undeclared...
The Issue: Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Agebox iKids-Growth (Day Formula) capsules Recalled by Agebox Due to...
The Issue: Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.