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. 2,341 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,341 in last 12 months

Showing 3340133420 of 47,970 recalls

Medical DeviceFebruary 5, 2016· Volcano Corporation

Recalled Item: Volcano R100 Sterile Equipment Cover Recalled by Volcano Corporation Due to...

The Issue: Volcano Corporation has identified that certain lot numbers of Volcano R-100...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Stryker Medical Division of Stryker Corporation

Recalled Item: Transport Stretcher Recalled by Stryker Medical Division of Stryker...

The Issue: The hydraulic jack assemblies (PN: 0753-002-101, 0753-002-070, 0753-002-001,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Volcano Corporation

Recalled Item: Volcano SpinVision Sterile Equip cover II Recalled by Volcano Corporation...

The Issue: Volcano Corporation has identified that certain lot numbers of Volcano R-100...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Stryker Medical Division of Stryker Corporation

Recalled Item: Prime Series Stretchers (Fifth Wheel Recalled by Stryker Medical Division of...

The Issue: The hydraulic jack assemblies (PN: 0753-002-101, 0753-002-070, 0753-002-001,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: (Stryker) AccuPlace Round Level Needle Guide Recalled by Stryker Instruments...

The Issue: During an evaluation of the product packaging, it was determined that there...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Abbott Vascular

Recalled Item: MitraClip Clip Delivery System Recalled by Abbott Vascular Due to Abbott...

The Issue: Abbott Vascular has recently received reports of cases on Clip Delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 50001 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare Diagnostic ADVIA Centaur Calibrator E- 6- Pack ()...

The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare Diagnostics ADVIA Centaur Calibrator E- 6- Pack Catalog...

The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare Diagnostics ADVIA Centaur Calibrator E - 2-Pack Catalog...

The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: (Stryker) AccuPlace Straight Level Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Draeger Medical, Inc.

Recalled Item: Evita Infinity V500 Ventilator Recalled by Draeger Medical, Inc. Due to The...

The Issue: The battery capacity of the optional PS500 power supply unit for the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 50000 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Smoked Pepperoni under the following labels:...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Trail Bologna under the following labels:...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Goetburg Summer Sausage under the following...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Dried Sticks Hot under the following Recalled by...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Dried Sausage Sticks under the following...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Summer Sausage under the following labels:...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Morphine Sulfate 1.5 mg/ml Recalled by Hartley Medical Center Pharmacy,...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund