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. 1,037 recalls have been distributed to Delaware in the last 12 months.
Showing 15481–15500 of 48,330 recalls
Recalled Item: Clio Strawberry Greek Yogurt Bars wrapped in a Chocolate Coating Recalled by...
The Issue: Possible metal fragments in Yogurt Bars
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DeRoyal Pacemaker Tray Pgybk Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Recalled...
The Issue: Device fail to detect Brady episodes, Pause (Asystole) episodes and PVC's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Heart Cath Procedure Pack Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac Dynamic software Recalled by Brainlab AG Due to Display of...
The Issue: Display of potential patient movement might be delayed to the user for high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Angio Cath Removal Tray Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORTEX UNLTRperc Percutaneous Dilation Tracheostomy Kit Recalled by Smiths...
The Issue: One lot number of a specific model of ULTRAperc Percutaneous Dilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: READYPREP CHG Recalled by Medline Industries Inc Due to Superpotent Drug:...
The Issue: Superpotent Drug: Product is above specification for active ingredient, 2%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diflorasone Diacetate Ointment USP Recalled by Teligent Pharma, Inc. Due to...
The Issue: Presence of Foreign Substance: Foreign particles observed during routine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atellica CH 930 Analyzer - multi-component system for in vitro Recalled by...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer - multi-component system for in vitro Recalled by...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer- multi-component system for in vitro diagnostic...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NATURE's ANSWER Coral Calcium Recalled by Bio-Botanica, Inc. Due to Product...
The Issue: Product contained cesium chloride, a New Dietary Ingredient
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: S3 MedSurg Bed - intended to support and transport patients Recalled by...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prime Fifth Wheel Stretcher-stretcher may be used for minor procedures...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proform- support surface is used to assist in the prevention Recalled by...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prime Big Wheel Stretcher-used as a short-term outpatient clinical...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S3 MedSurg Bed - intended to support and transport patients Recalled by...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.