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 2998130000 of 47,970 recalls

Medical DeviceDecember 21, 2016· PerkinElmer Health Sciences, Inc.

Recalled Item: Program Update Package AutoDELFIA¿ 3.0 Recalled by PerkinElmer Health...

The Issue: AutoDELFIA System with Version 3.0 Software: Potential plate loading failures

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

Class III — Low RiskOngoing
Medical DeviceDecember 21, 2016· PerkinElmer Health Sciences, Inc.

Recalled Item: DELFIA¿ PC with V3.0 Software Recalled by PerkinElmer Health Sciences, Inc....

The Issue: AutoDELFIA System with Version 3.0 Software: Potential plate loading failures

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

Class III — Low RiskOngoing
Medical DeviceDecember 20, 2016· Becton Dickinson & Company

Recalled Item: Eclipse Hypodermic Needle Recalled by Becton Dickinson & Company Due to BD...

The Issue: BD is initiating a Product Advisory for the Eclipse Hypodermic Needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2016· Zimmer Biomet, Inc.

Recalled Item: Comprehensive Reverse Shoulder System Humeral Tray Model 115340 Recalled by...

The Issue: Higher than anticipated rate of fracturing due to design. Risk of revision...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Na+ Slides Recalled by Ortho-Clinical Diagnostics Due to There is a...

The Issue: There is a potential for biased results to be generated over the 10 day...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2016· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Connect Diabetes Management App Recalled by Roche Diabetes Care,...

The Issue: iOS and Android: Under certain conditions the affected app versions may...

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

Class II — Potential Health HazardOngoing
FoodDecember 20, 2016· Herr Foods, Inc.

Recalled Item: Smoked Chipotle Flavored Kettle Cooked Potato Chips 2.625 oz and 8.0 oz...

The Issue: Herrs Foods is announcing a product recall on Chipotle flavored Kettle...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 20, 2016· Herr Foods, Inc.

Recalled Item: Dried Smoke Chipotle Flavored Kettle Cooked Potato Chips 2.0 oz. Recalled by...

The Issue: Herrs Foods is announcing a product recall on Chipotle flavored Kettle...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: buPROPion Hydrochloride Extended-release Tablets Recalled by Sun...

The Issue: Failed Dissolution Specifications; 18 month stability time point

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

Class III — Low RiskOngoing
Refund
DrugDecember 20, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: buPROPion Hydrochloride Extended-release Tablets Recalled by Sun...

The Issue: Failed Dissolution Specifications; 18 month stability time point

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

Class III — Low RiskOngoing
Refund
DrugDecember 20, 2016· Mylan LLC.

Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...

The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2016· Mylan LLC.

Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...

The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2016· Mylan LLC.

Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...

The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2016· Accord Healthcare, Inc.

Recalled Item: Lisinopril tablets Recalled by Accord Healthcare, Inc. Due to Failed...

The Issue: Failed tablet/capsule specification: missing break line on the 5mg tablet.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2016· Mylan LLC.

Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...

The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 19, 2016· Apotex Inc.

Recalled Item: Aripiprazole Tablets Recalled by Apotex Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: Product may not meet specifications throughout shelf life.

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 19, 2016· Zimmer Biomet, Inc.

Recalled Item: RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall...

The Issue: Product complaints indicated that the part and lot numbers on the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· Zimmer Biomet, Inc.

Recalled Item: Active Articulation ArComXL Polyethylene Bearings Active Articulation...

The Issue: Product complaints indicated that the part and lot numbers on the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· GE OEC Medical Systems, Inc

Recalled Item: OEC 9800. MDL Numbers: D222250 Recalled by GE OEC Medical Systems, Inc Due...

The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2016· Beckman Coulter Inc.

Recalled Item: DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter Inc....

The Issue: Beckman Coulter has determined that additional clarification for the Blast...

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

Class II — Potential Health HazardOngoing