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 46321–46340 of 48,330 recalls
Recalled Item: Kellogg's Variety and Assortment Packs containing Frosted/ Unfrosted Mini...
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: American Vines band Natural Vines Black Soft Licorice Twists Recalled by...
The Issue: Firm's internal sampling of the product found elevated levels of lead in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kellogg's Frosted Mini Wheats Recalled by Kellogg Company Due to This...
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: Biomet Polaris 5.5 Button Lock Screw Inserter. Catalog number 14-500178...
The Issue: Broken screw insertor hardness was measured and found to be below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENTANA (a member of the Roche Group) DISCOVERY ULTRA Recalled by Ventana...
The Issue: Potential for a waste fluid overflow condition to accur while running...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is Full OSSEOTITE 2 Tapered Certain Implant Recalled by Biomet 3i,...
The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm Cancellous Bone Screw Intended to be used for the Recalled by Encore...
The Issue: A product complaint was received where a size 20 screw was labeled as size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Philips Medical Systems...
The Issue: Philips is issued a Field Change Order to update Extended Brilliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3 PORT "OFF" MANIFOLD w/WASTE BAG Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical, Inc. has identified a potential comingling of components where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is Full OSSEOTITE Parallel Walled Certain Implant Recalled by Biomet...
The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pro Time Microcoagulation System/ Pro Time 3 Cuvette Recalled by...
The Issue: Some Pro Time3 Test Cuvettes within a specified lot range may recover lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes External Fixation System Tube to Tube Clamp Recalled by Synthes USA...
The Issue: The insert provided with the product for the specific lot number indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENTANA (a member of the Roche Group) BenchMark ULTRA Recalled by Ventana...
The Issue: Potiential for a waste fluid overflow condition to accur while running...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Late July Organic Mini Peanut Butter Sandwich Crackers packaged in Recalled...
The Issue: Organic Mini Peanut Butter Sandwich Crackers are recalled due to Sunland...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fairytale Brownies Brand Peanut Butter Brownies Recalled by Fairytale...
The Issue: The firm initiated voluntarily recall because the products contains peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fairytale Brand Peanut Butter Sprites Recalled by Fairytale Brownies, Inc...
The Issue: The firm initiated voluntarily recall because the products contains peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fairytale Brownies Brand Peanut Butter Cookies Recalled by Fairytale...
The Issue: The firm initiated voluntarily recall because the products contains peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lemon Hand Sanitizing Wipes [n-alkyl dimethyl benzyl ammonium chloride...
The Issue: CGMP Deviations: The products were manufactured with raw material which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Quetiapine Fumarate Tablets Recalled by Dr. Reddy's...
The Issue: Failed USP Dissolution Test Requirements: During analysis of long term...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CYANOCOBALAMIN INJECTION Recalled by Fresenius Kabi USA, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility: Glass vials may have finish fractures and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.