Product Recalls in Rhode Island

Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,263 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,263 in last 12 months

Showing 4518145200 of 47,970 recalls

FoodFebruary 19, 2013· Blue Planet Foods, Inc.

Recalled Item: Heartland Recalled by Blue Planet Foods, Inc. Due to Blue Planet products...

The Issue: Blue Planet products that contain the two recalled Dakota Specialty Milling...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 19, 2013· Bimbo Bakeries Usa

Recalled Item: Stroehmann Dutch Country 100% Whole Grain Bread Recalled by Bimbo Bakeries...

The Issue: Firm has initiated a voluntary recall due to the possible presence of...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 19, 2013· Hospira Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2013· Remel Inc

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.

Class III — Low RiskOngoing
Medical DeviceFebruary 19, 2013· Tecan US, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

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.

Class II — Potential Health HazardOngoing
DrugFebruary 18, 2013· Hospira Inc.

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.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 18, 2013· Ge Medical Systems Information T

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.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Ge Healthcare It

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.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· GE Healthcare

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.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

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.

Class II — Potential Health HazardOngoing
DrugFebruary 15, 2013· Warner Chilcott Company LLC

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.

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2013· Warner Chilcott Company LLC

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.

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2013· Warner Chilcott Company LLC

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.

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2013· Dr Reddys Laboratories Tennessee LLC

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.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2013· Hospira Inc.

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.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2013· Kellogg Company

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.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2013· Decoty Coffee Company, Inc

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.

Class I — Serious Health HazardOngoing
Refund