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. 2,298 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,298 in last 12 months

Showing 4156141580 of 47,970 recalls

DrugJanuary 24, 2014· Teva Pharmaceuticals USA

Recalled Item: Teva Hydroxyzine Pamoate Capsules Recalled by Teva Pharmaceuticals USA Due...

The Issue: CGMP Deviations: Hydroxyzine Pamoate Capsules, USP, 25 mg were manufactured...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 24, 2014· Hospira Inc.

Recalled Item: Plum XL Recalled by Hospira Inc. Due to There is the potential for the door...

The Issue: There is the potential for the door roller assembly on the Plum LifeCare...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Hospira Inc.

Recalled Item: Plum XL3 Multi line Infusion System Recalled by Hospira Inc. Due to There is...

The Issue: There is the potential for the door roller assembly on the Plum LifeCare...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Hospira Inc.

Recalled Item: LifeCare 5000 Pump (Plum 1.6) infusion pump Recalled by Hospira Inc. Due to...

The Issue: There is the potential for the door roller assembly on the Plum LifeCare...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Clarity Medical Systems Inc

Recalled Item: RetCam 3 Recalled by Clarity Medical Systems Inc Due to Software anomaly for...

The Issue: Software anomaly for RetCam 3, RetCam Shuttle and RetCam Portable with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Carestream Health Inc.

Recalled Item: Model Kodak 2100 Intraoral X-Ray System Recalled by Carestream Health Inc....

The Issue: Carestream received problem reports relating to apparent early failure of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Carestream Health Inc.

Recalled Item: Model Kodak 2200 Intraoral X-Ray System Recalled by Carestream Health Inc....

The Issue: Carestream received problem reports relating to apparent early failure of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Hologic, Inc

Recalled Item: NovaSure Impedance Controlled Endometrial Ablation System Radiofrequency...

The Issue: NovaSure Radiofrequency Control Units may not meet a requirement of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Model: 861290 The HeartStart...

The Issue: HeartStart XL+ battery charge time to 100% capacity at 35¿C (95¿F) is...

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

Class II — Potential Health HazardOngoing
FoodJanuary 23, 2014· Araya, Inc

Recalled Item: Marshmallow in the following flavors: chocolate Recalled by Araya, Inc Due...

The Issue: Product may contain undeclared allergens

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 23, 2014· Araya, Inc

Recalled Item: Chocolate Gift Boxes: SC 6 Oreos Recalled by Araya, Inc Due to Undeclared...

The Issue: Product may contain undeclared allergens

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 23, 2014· Araya, Inc

Recalled Item: Dry fruits covered in chocolate in the following flavors: orange peel...

The Issue: Product may contain undeclared allergens

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 23, 2014· Araya, Inc

Recalled Item: Chocolate S'mores Araya Artisan Chocolate: 1545 W Grand Parkway S Recalled...

The Issue: Product may contain undeclared allergens

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 23, 2014· Araya, Inc

Recalled Item: Gourmet Bar in the following flavors: bacon Recalled by Araya, Inc Due to...

The Issue: Product may contain undeclared allergens

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 23, 2014· Atricure Inc

Recalled Item: Reusable Clip Applier Manufactured by AtriCure Recalled by Atricure Inc Due...

The Issue: The firm was notified by a customer of a cracked spring in the handle of the...

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

Class II — Potential Health HazardOngoing
DrugJanuary 22, 2014· Fresenius Kabi USA, LLC

Recalled Item: Heparin Sodium Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Subpotent; 18 month time point

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 22, 2014· CareFusion 303, Inc.

Recalled Item: SmartSite Needleless Connector Recalled by CareFusion 303, Inc. Due to...

The Issue: CareFusion is recalling the SmartSite Needlefree Connector, model number...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2014· Golden Technologies, Inc.

Recalled Item: Buzzaround XL scooters' Product Usage: mobility Recalled by Golden...

The Issue: Buzzaround XL scooters' front to rear lockup can become unintentionally...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2014· Dako North America Inc.

Recalled Item: Product Name: HER2 CISH pharmDx Kit Catalog/Model number: SK109 Recalled by...

The Issue: Dako has initiated a recall of HER2 CISH pharmDxTM Kit because weak red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2014· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA Multical. ABX PENTRA N Control. ABX PENTRA P Recalled by Horiba...

The Issue: HORIBA Medical is informing all ABX PENTRA MultiCal, N Control, and P...

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

Class II — Potential Health HazardOngoing