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. 2,560 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,560 in last 12 months

Showing 27212740 of 47,970 recalls

DrugMarch 11, 2025· Fruit Of The Earth, Inc.

Recalled Item: CVS Health Concealing Acne Treatment Cream Recalled by Fruit Of The Earth,...

The Issue: Chemical contamination: presence of benzene

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 11, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Glenmark Pharmaceuticals...

The Issue: CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 11, 2025· FDC Limited

Recalled Item: Ciprofloxacin Ophthalmic Solution USP Recalled by FDC Limited Due to...

The Issue: Defective container: Unable to get the solution out of the bottle as the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 11, 2025· Fruit Of The Earth, Inc.

Recalled Item: Walgreens Maximum Strength Tinted Acne Treatment Cream 10% Benzoyl...

The Issue: Chemical contamination: presence of benzene

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 11, 2025· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK (Name Recalled by CareFusion 303, Inc. Due to Users trying...

The Issue: Users trying to restock a single bin location of an automated dispensing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2025· Bard Access Systems, Inc.

Recalled Item: BD 4 Fr Single-Lumen PowerPICC Catheters Recalled by Bard Access Systems,...

The Issue: Catheters indicated for short-or-long term access to the central venous...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 11, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower Recalled by CareFusion...

The Issue: Due to a software bug, automated dispensing cabinet is unable to calculate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Revised C Reactive Protein (RCRP) Recalled by Siemens Healthcare...

The Issue: Incorrect software flagging may occur for the assay that may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2025· Medtronic Xomed, Inc.

Recalled Item: NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0 Recalled by...

The Issue: Nerve Monitoring System with certain software versions has potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2025· Philips North America Llc

Recalled Item: Philips DXR System Recalled by Philips North America Llc Due to Potential...

The Issue: Potential for collimator to fall as a result of incorrect installation.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2025· Maquet Cardiovascular, LLC

Recalled Item: Maquet VH-3010 Power Supply. Used to deliver power to the Recalled by Maquet...

The Issue: Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2025· Philips North America Llc

Recalled Item: Philips DXR System Recalled by Philips North America Llc Due to Potential...

The Issue: Potential for collimator to fall as a result of incorrect installation.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2025· Straumann USA LLC

Recalled Item: TLX/TLC SP Guided Implant Driver Recalled by Straumann USA LLC Due to The...

The Issue: The devices are missing the laser marked depth markings.

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

Class II — Potential Health HazardOngoing
DrugMarch 7, 2025· Direct Rx

Recalled Item: Duloxetine D/R Recalled by Direct Rx Due to CGMP Deviations: Presence of...

The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Direct Rx

Recalled Item: Duloxetine D/R Recalled by Direct Rx Due to CGMP Deviations: Presence of...

The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· ASEGUA THERAPEUTICS LLC

Recalled Item: Sofosbuvir and Velpatasvir Recalled by ASEGUA THERAPEUTICS LLC Due to...

The Issue: Defective Container: blister packs not properly sealed resulting in tablets...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Exela Pharma Sciences LLC

Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...

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
DrugMarch 7, 2025· Mylan Institutional, Inc.

Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...

The Issue: Super-Potent Drug: Out of specification potency results were obtained.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Slate Run Pharmaceuticals

Recalled Item: Cinacalcet Hydrochloride Tablets 60 mg Recalled by Slate Run Pharmaceuticals...

The Issue: CGMP deviations: The presence of nitrosamine impurity above the acceptable...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Mylan Institutional, Inc.

Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...

The Issue: Super-Potent Drug: Out of specification potency results were obtained.

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

Class II — Potential Health HazardOngoing
Refund