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. 1,667 recalls have been distributed to Delaware in the last 12 months.
Showing 46301–46320 of 48,330 recalls
Recalled Item: All Non Sterile Products manufactured by NECC (New England Compounding...
The Issue: GMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All Sterile Products manufactured by NECC (New England Compounding Center)...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Starbucks Protein Bistro Box Recalled by Flying Food Group, Inc. Due to...
The Issue: Starbucks Protein Bistro Boxes contain Honey Peanut Butter Squeeze Packs...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate Peanut Butter Cup Gelato. The product was distributed to Recalled...
The Issue: Talenti Gelato is recalling Talenti Chocolate Peanut Butter Cup Gelato. The...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lactated Ringer's and 5% Dextrose Injection Recalled by Hospira Inc. Due to...
The Issue: Non-Sterility: One confirmed customer report that product contained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colloidal Silver Recalled by Earthborn Products, Inc. Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA: This product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The touchscreen display (model 94267) designed for use with the Recalled by...
The Issue: Potential failure of Spacelabs Healthcare Touchscreen Display, Model 94267...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo WorkFlow SLR Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Under certain conditions, when using the Search functionality, the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle3 VCC P/N 4598 001 41341 REV A Recalled by Philips Medical Systems...
The Issue: Philips Medical Systems Cleveland), Inc. is recalling Pinnacle3 Virtual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ranawat/Burnstein Acetabular Shell 54mm/Limited Holes/Porous Coated is a...
The Issue: The color code on label conflicts with the liner size (liner size 24 should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine HCl Injection Recalled by Hospira, Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Report of a vial containing visible...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUITONI brand Spinach & Portobello Mushroom All Natural Ravioli Recalled by...
The Issue: BUITONI Spinach & Portobello Mushroom All Natural Ravioli may instead...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Moexipril HCl Tablets 7.5mg Recalled by Paddock Laboratories, LLC Due to...
The Issue: Paddock Laboratories, LLC are recalling one lot (2012028142) of Moexipril...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: West Nile Virus IgG DxSelect" kit Catalog No. EL0300G Kit Lots 122150...
The Issue: The firm recalled due to higher reactivity with some samples in the effected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Repeater Pump Recalled by Baxa Corporation Due to The firm is issuing a...
The Issue: The firm is issuing a field correction to the operators manual included with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD CYCLESURE 24 Biological Indicator (BI) product Recalled by Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling all lots of Sterrad...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Cardio Imaging 5.0 is a software only Picture Archiving Recalled...
The Issue: GE Healthcare is aware of a potential safety risk where an image labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Case Carton: BD Oral Dispensing Syringe 1 mL Clear with Tip Cap BD Recalled...
The Issue: BD received a complaint report for mixed syringe tips (oral and non-oral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kellogg's Mini Wheats Recalled by Kellogg Company Due to This voluntary...
The Issue: This voluntary recall is initiated due to the possible presence of fragments...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Canadian Product: Kellogg's Mini Wheats Recalled by Kellogg Company Due to...
The Issue: This voluntary recall is initiated due to the possible presence of fragments...
Recommended Action: Do not consume. Return to store for a refund or discard.