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. 2,351 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,351 in last 12 months

Showing 3070130720 of 47,970 recalls

Medical DeviceSeptember 30, 2016· Bayer Healthcare

Recalled Item: PET Infusion Pump Recalled by Bayer Healthcare Due to The Source...

The Issue: The Source Administration Sets (SAS) used with the Medrad Intego PET...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Mako Surgical Corporation

Recalled Item: Stryker Restoris RIO Reamer Handle Recalled by Mako Surgical Corporation Due...

The Issue: Failure of the Offset Cup Reamer Handle not engaging its mating components.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Thayer Medical Corporation

Recalled Item: Thayer MiniSpacer Dual Spray MDI Adapter Counter Incrementing Actuator with...

The Issue: The insert and case label description of the device incorrectly reads...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Sorin Group USA, Inc.

Recalled Item: The ORCHESTRA PLUS Programmer A portable device Recalled by Sorin Group USA,...

The Issue: Sorin Group USA, Inc. announces a voluntary field action for the ORCHESTRA...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Aptio Automation Modules Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Possible overheating of power cord plugs used to connect to FlexLab and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Sorin Group USA, Inc.

Recalled Item: The ORCHESTRA Programmer A portable device Recalled by Sorin Group USA, Inc....

The Issue: Sorin Group USA, Inc. announces a voluntary field action for the ORCHESTRA...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: FlexLab Automation Modules Recalled by Siemens Healthcare Diagnostics, Inc....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Covidien LLC

Recalled Item: Professional Hospital Supply Recalled by Covidien LLC Due to Added...

The Issue: Added Instructions for Use: After application, inspect the Light Glove for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Covidien LLC

Recalled Item: Covidien Devon Light Glove packaged in sterile surgical kits : Recalled by...

The Issue: Added Instructions for Use: After application, inspect the Light Glove for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Covidien LLC

Recalled Item: Covidien Devon Light Glove sub-assembly non-sterile For Kit Packers Product...

The Issue: Added Instructions for Use: After application, inspect the Light Glove for...

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

Class II — Potential Health HazardOngoing
DrugSeptember 28, 2016· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Impurities/Degradation Specifications: out of specification result...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 28, 2016· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Impurities/Degradation Specifications: out of specification result...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 28, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Yankee Bourbon BBQ Sauce. 19oz glass bottles and 1 gallon...

The Issue: Products contain soy ingredients not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 28, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Apple Riesling Salsa. 21oz glass bottles and 1 Recalled by...

The Issue: Products contain yellow#5 ingredients not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 28, 2016· Brownwood Farms

Recalled Item: Brownwood Farms BBQ Mustard Glaze. 11oz glass bottles and 1 Recalled by...

The Issue: Products contain soy ingredients not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 28, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Jalapeno Cherry Butter. 12oz glass bottles and 1 gallon....

The Issue: Products contain yellow#5 ingredients not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 28, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Jalapeno Cherry Salsa. 21oz glass bottles and 1 Recalled by...

The Issue: Products contain yellow#5 ingredients not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 28, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Peach Salsa. 17oz glass bottles. Private labels: Bowers...

The Issue: Products contain yellow#5 ingredients not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 28, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Cherry BBQ Sauce. 21oz glass bottles Recalled by Brownwood...

The Issue: Products contain soy ingredients not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing