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 27612780 of 27,456 recalls

Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: LifeVent EVO2. Model Number: SP2100X26B. Intended for invasive and...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Ventilator. Model Number DS2000X11B. Intended for...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo O2. Model Numbers: FP2100X10 Recalled by Philips Respironics,...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· DRG International, Inc.

Recalled Item: DRG:HYBRiD-XL Insulin. Model/Catalog Number: HYE-5361 Recalled by DRG...

The Issue: The user of the assay may either face a failure message during...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo. Model Numbers: DS2110X11B Recalled by Philips Respironics, Inc....

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy EV300. Model Numbers: DS2200X11B Recalled by Philips Respironics,...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Garbin Evo. Model Number: LD2110X23B. Intended for invasive and non-invasive...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Zenition 50 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Potential for the Mains Control Unit board fuse may blow out during system...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2024· St. Jude Medical

Recalled Item: CARDIOMEMS HF PRESSURE MEASUREMENT SYSTEM CardioMEMSTM HF System Patient...

The Issue: As a result of a cloud data migration of Patient and Hospital Electronic...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2024· St. Jude Medical

Recalled Item: CARDIOMEMS HF PRESSURE MEASUREMENT SYSTEM CardioMEMSTM HF System Hosptial...

The Issue: As a result of a cloud data migration of Patient and Hospital Electronic...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Caire, Inc.

Recalled Item: CAIRE FreeStyle Comfort portable oxygen concentrator Recalled by Caire, Inc....

The Issue: Potential failure of affected units to recharge the battery of the oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Push-Button Recalled...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Recalled by Stryker...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Non coated 70 mm Recalled by...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Caire, Inc.

Recalled Item: CAIRE FreeStyle Comfort portable oxygen concentrator Recalled by Caire, Inc....

The Issue: Potential failure of affected units to recharge the battery of the oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Caire, Inc.

Recalled Item: CAIRE FreeStyle Comfort portable oxygen concentrator Recalled by Caire, Inc....

The Issue: Potential failure of affected units to recharge the battery of the oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Rocker-Switch...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing