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. 2,314 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,314 in last 12 months

Showing 3712137140 of 47,970 recalls

Medical DeviceMarch 25, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Universal Charger Product Usage: The Stryker Universal Battery Charger is...

The Issue: The Stryker Universal Battery Charger is not transmitting usage data to the...

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

Class III — Low RiskOngoing
Medical DeviceMarch 25, 2015· Nidek Inc

Recalled Item: Endophotocoagulation Delivery 4EP-1 of GYC-1000 Green Laser Photocoagulator...

The Issue: Accessories to the GYC-1000 laser were missing Laser Aperture labels.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2015· Nidek Inc

Recalled Item: Dual Delivery 4DD-1 of GYC-1000 Green Laser Photocoagulator system GYC4DD-1:...

The Issue: Accessories to the GYC-1000 laser were missing Laser Aperture labels.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2015· The Anspach Effort, Inc.

Recalled Item: Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number:...

The Issue: The potential exists for the Oscillating Saw Attachment to disengage from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton-G5 Ventilators with software versions V2.40/2.41 Catalog numbers...

The Issue: Customer reports that the ventilator display can freeze. Ventilation...

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

Class II — Potential Health HazardOngoing
DrugMarch 24, 2015· Nomax Inc

Recalled Item: Fluorescein Sodium Ophthalmic Strips USP Recalled by Nomax Inc Due to Failed...

The Issue: Failed Content Uniformity Specifications: The product may not meet finished...

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

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2015· Nomax Inc

Recalled Item: Fluorescein Sodium Ophthalmic Strips USP Recalled by Nomax Inc Due to Failed...

The Issue: Failed Content Uniformity Specifications: The product may not meet finished...

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

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2015· Nomax Inc

Recalled Item: Rose Bengal GloStrips (rose bengal) Ophthalmic Strips USP Recalled by Nomax...

The Issue: Failed Content Uniformity Specifications: The product may not meet finished...

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

Class III — Low RiskOngoing
Refund
DrugMarch 23, 2015· Mylan Institutional LLC

Recalled Item: Gemcitabine for Injection Recalled by Mylan Institutional LLC Due to...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 23, 2015· Mylan Institutional LLC

Recalled Item: Gemcitabine for Injection Recalled by Mylan Institutional LLC Due to...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 23, 2015· Mylan Institutional LLC

Recalled Item: Gemcitabine for Injection Recalled by Mylan Institutional LLC Due to...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 23, 2015· Baxter Healthcare Corp

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp Due to...

The Issue: Lack of Assurance of Sterility; increased complaints received for leaks

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2015· Baxter Healthcare Corp

Recalled Item: Clinimix E 5/20 sulfite-free (5% amino-acid with electrolytes in 20%...

The Issue: Lack of Assurance of Sterility; increased complaints received for leaks

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 23, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Lipase Reagent Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens internal investigation confirmed that current contamination...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2015· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Fem-Flex II Femoral Arterial Cannula 8 Recalled by...

The Issue: Edwards Lifesciences is recalling Fem-Flex II Pediatric Femoral Arterial...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Homocysteine test system - Homocysteine Reagent. 05385415190 Recalled by...

The Issue: Customers complained about under-recovery of non-Roche controls and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2015· Philips Electronics North America Corporation

Recalled Item: Philips DigitalDiagnost Release 4.0.3 Recalled by Philips Electronics North...

The Issue: The system is designed to emit a beep upon termination of an exposure....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2015· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems Recalled by...

The Issue: Medtronic is conducting a voluntary recall of all former Covidien Trellis 6...

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

Class II — Potential Health HazardOngoing
FoodMarch 23, 2015· Carmel Food Group, Inc.

Recalled Item: Rising Moon Organics Garlic and Veggie Ravioli Recalled by Carmel Food...

The Issue: Firm was notified by supplier of spinach and used in manufacturing showed...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 23, 2015· Carmel Food Group, Inc.

Recalled Item: Rising Moon Organics Spinach & Cheese Ravioli Recalled by Carmel Food Group,...

The Issue: Firm was notified by supplier of spinach and used in manufacturing showed...

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

Class II — Potential Health HazardOngoing
Refund