Product Recalls in Connecticut
Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,739 recalls have been distributed to Connecticut in the last 12 months.
Showing 48221–48240 of 51,038 recalls
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: 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: 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: 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: 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: 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: 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: 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: 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: Femhrt (norethindrone acetate and ethinyl estradiol) tablets Recalled by...
The Issue: Chemical contamination: Firm's inspection discovered the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Femhrt (norethindrone acetate and ethinyl estradiol) tablets Recalled by...
The Issue: Chemical contamination: Firm's inspection discovered the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Jevantique (norethindrone acetate and ethinyl estradiol) tablets Recalled by...
The Issue: Chemical contamination: Firm's inspection discovered the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amoxicillin for Oral Suspension Recalled by Dr Reddys Laboratories Tennessee...
The Issue: Microbial Contamination of Non-Sterile Products: Suspensions made from these...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: METRONIDazole Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: There is the potential for the solution to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Taco Seasoning Recalled by Decoty Coffee Company, Inc Due to Undeclared...
The Issue: DeCoty Coffee Company of San Angelo, Texas is recalling its 1.25lb and...
Recommended Action: Do not consume. Return to store for a refund or discard.
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.