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. 907 recalls have been distributed to Delaware in the last 12 months.
Showing 45501–45520 of 48,330 recalls
Recalled Item: Remel X/pect Flu A&B Control Swabs Recalled by Remel Inc Due to Flu A+...
The Issue: Flu A+ Control Swabs incorrectly give Flu A- results when used for quality...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tecan Freedom EVO with Touch Tools Suite Version 3.0 The Recalled by Tecan...
The Issue: WIth TouchTools 3.0 after the execution of a Rich User Prompt in Display and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic DPL Single Stage Venous Cannula with Metal Tip Recalled by...
The Issue: Potential for uncharacteristically rough metal edges to occur along the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lamisil AT Cream (terbinafine hydrochloride 1% antifungal) Recalled by...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novartis Lamisil AT Cream Recalled by Novartis Consumer Health Due to...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novartis Lamisil AT Cream for Jock Itch (terbinafine hydrochloride 1%...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Target Up & Up Recalled by Novartis Consumer Health Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Voltaren Gel (diclofenac sodium topical gel) 1% Recalled by Novartis...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minibore Extension Set Recalled by Hospira Inc. Due to Hospira, Inc. is...
The Issue: Hospira, Inc. is voluntarily recalling one lot of list 14699-28, Minibore...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imagecast PACS with Centricity RIS-IC versions prior to 10.6 Update Recalled...
The Issue: A software defect was discovered that causes images to be out of context...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS Web Diagnostic (WebDX) by GE Healthcare Dynamic Imaging...
The Issue: It was reported from a complaint that study category labels of "Prior" and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...
The Issue: Using Merge Exam in single Study Mode may result in Missing Study Record...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: The product is being recall due to the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITEK 2 XL computer system when equipped with the following Recalled by...
The Issue: There is a potential to link an isolate result to the wrong patient and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 Compact computer system when equipped with the following Recalled by...
The Issue: There is a potential to link an isolate result to the wrong patient and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 60 computer system when equipped with the following Recalled by...
The Issue: There is a potential to link an isolate result to the wrong patient and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX Micros IM2 Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...
The Issue: Horiba Medical is recalling ABX Micros IM2 Data Management System because it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...
The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...
The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kellogg's Special K Red Berries Recalled by Kellogg Company Due to A limited...
The Issue: A limited amount of Kellogg's Special K, Red Berries is being recalled due...
Recommended Action: Do not consume. Return to store for a refund or discard.