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 18411860 of 47,970 recalls

FoodJuly 11, 2025· DANONE US LLC

Recalled Item: YoCrunch Lowfat Yogurt with Toppers Recalled by DANONE US LLC Due to Foreign...

The Issue: Foreign material (plastic pieces)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2025· DANONE US LLC

Recalled Item: YoCrunch Low Fat Yogurt with Toppers Recalled by DANONE US LLC Due to...

The Issue: Foreign material (plastic pieces)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2025· DANONE US LLC

Recalled Item: YoCrunch Low Fat Yogurt with Toppers Recalled by DANONE US LLC Due to...

The Issue: Foreign material (plastic pieces)

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 11, 2025· Onkos Surgical, Inc.

Recalled Item: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to...

The Issue: Unidentified substance of unknown impact was identified on devices during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2025· Flexicare Medical (Dongguan) Ltd.

Recalled Item: BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handle Recalled by...

The Issue: Laryngoscope handles may not illuminate as intended.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2025· Remel, Inc

Recalled Item: Blood/MacConkey Biplate 100/PK Recalled by Remel, Inc Due to Potential...

The Issue: The products may contain surface and subsurface contamination of Listeria...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2025· Remel, Inc

Recalled Item: Strep Selective II Agar Recalled by Remel, Inc Due to Potential Listeria...

The Issue: The products may contain surface and subsurface contamination of Listeria...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2025· Remel, Inc

Recalled Item: Blood Agar Recalled by Remel, Inc Due to Potential Listeria Contamination

The Issue: The products may contain surface and subsurface contamination of Listeria...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2025· mo-Vis BVBA

Recalled Item: Multi Joystick R-net. Electrical wheelchair component. Recalled by mo-Vis...

The Issue: Devices with firmware versions 2.3 and lower may experience timing...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 10, 2025· Biofire Defense

Recalled Item: FilmArray NGDS Warrior Panel NGDS-ASY-0007 is a qualitative Recalled by...

The Issue: FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2025· mo-Vis BVBA

Recalled Item: IDM-MICRO-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...

The Issue: Devices with firmware versions 2.3 and lower may experience timing...

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

Class I — Serious Health HazardOngoing
DrugJuly 10, 2025· A.P. Deauville, LLC

Recalled Item: Shave and Skincare Power Stick Original Nourishing Invisible Protection...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 10, 2025· A.P. Deauville, LLC

Recalled Item: Beauty & Skincare Power Stick original nourishing invisible protection...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 10, 2025· A.P. Deauville, LLC

Recalled Item: Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 10, 2025· mo-Vis BVBA

Recalled Item: Micro Joystick R-net. Electrical wheelchair component. Recalled by mo-Vis...

The Issue: Devices with firmware versions 2.3 and lower may experience timing...

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

Class I — Serious Health HazardOngoing
DrugJuly 10, 2025· Pfizer Inc.

Recalled Item: Bicillin L-A (penicillin G benzathine injectable suspension) Recalled by...

The Issue: CGMP Deviations; particulates identified during visual inspection

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 10, 2025· Pfizer Inc.

Recalled Item: Bicillin L-A (penicllin G benzathine injectable suspension) Recalled by...

The Issue: CGMP Deviations; particulates identified during visual inspection

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 10, 2025· mo-Vis BVBA

Recalled Item: IDM-ARLITE-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due...

The Issue: Devices with firmware versions 2.3 and lower may experience timing...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 10, 2025· CareFusion 303, Inc.

Recalled Item: Description/ PYXIS MEDBANK MINI 1FH-1FM/169-137 Recalled by CareFusion 303,...

The Issue: Reports of delayed access to medication in automated dispensing cabinets...

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

Class III — Low RiskOngoing
Medical DeviceJuly 10, 2025· Beckman Coulter, Inc.

Recalled Item: Access Thyroglobulin assay Recalled by Beckman Coulter, Inc. Due to Access...

The Issue: Access Thyroglobulin reagent lot 439163 may generate erroneously high...

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

Class II — Potential Health HazardOngoing