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 19411960 of 47,970 recalls

Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: S8-3t Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: c5-1 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: D5cwc Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: Transducer C10-3v Transducer Probe Recalled by Philips Ultrasound, Inc Due...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: L12-3 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: Mini Multi TEE Transducer Probe Recalled by Philips Ultrasound, Inc Due to...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: S4-1 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: V6-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: C9-4 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: L12-5 50 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: V9-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: XL14-3 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: X8-2t Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: C9-3io Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: L11-3 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: OMNI III TEE Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Orascoptic Surgical Acuity

Recalled Item: Orascoptic Superior Visualization Custom loupes with Dragonfly frames...

The Issue: Due to complaints, loupe nose pads containing nickel may cause an allergic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: D2TCD Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: C5-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: L15-7IO TRANSDUCER Transducer Probe Recalled by Philips Ultrasound, Inc Due...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing