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. 2,526 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,526 in last 12 months

Showing 66416660 of 27,456 recalls

Medical DeviceMarch 1, 2023· Terumo Cardiovascular Systems Corporation

Recalled Item: CAPIOX RX15 Hollow Fiber Oxygenator Recalled by Terumo Cardiovascular...

The Issue: Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Philips Respironics, Inc.

Recalled Item: Trilogy EV300 Portable Electric Ventilator Recalled by Philips Respironics,...

The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2023· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Portable Electric Ventilator Recalled by Philips...

The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2023· Stryker Corporation

Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 34X4...

The Issue: Not able to achieve desired pressure and not holding pressure result from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Stryker Corporation

Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 34X4...

The Issue: Not able to achieve desired pressure and not holding pressure result from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Philips Respironics, Inc.

Recalled Item: Trilogy Evo O2 and LifeVentEVO2 Portable Electric Ventilator Recalled by...

The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2023· Stryker Corporation

Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 18X4...

The Issue: Not able to achieve desired pressure and not holding pressure result from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Elekta Instrument AB

Recalled Item: Instructions for Use for the following Leksell Stereotactic System and...

The Issue: The incorrect IFU was distributed with the devices.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Atrium Medical Corporation

Recalled Item: Express Mini 500 Dry Seal Chest Drain Recalled by Atrium Medical Corporation...

The Issue: The Instructions for Use (IFU) for the Pneumostat Chest Drain Valve and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Stryker Sustainability Solutions

Recalled Item: Color Cuff Single Port Recalled by Stryker Sustainability Solutions Due to...

The Issue: Increased incidence of disposable tourniquet cuffs "not able to achieve...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Atrium Medical Corporation

Recalled Item: Atrium Pneumostat Chest Drain Valve Recalled by Atrium Medical Corporation...

The Issue: The Instructions for Use (IFU) for the Pneumostat Chest Drain Valve and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2023· Omega Medical Imaging, Inc.

Recalled Item: Omega Medical Imaging Elevating Monitor Suspension Recalled by Omega Medical...

The Issue: An actuator separated from the pivot mechanism on a lower monitor boom...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2023· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to APLS IgM reagent...

The Issue: APLS IgM reagent kits were packaged with the incorrect conjugate, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2023· Bard Peripheral Vascular Inc

Recalled Item: Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM Recalled by...

The Issue: The external diameter of the biopsy instrument is larger than the internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2023· Elekta Inc

Recalled Item: Monaco RTP System. Used to make treatment plans for patients Recalled by...

The Issue: Re-optimization, after adding contours without forced density outside the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2023· FUJIFILM Healthcare Americas Corporation

Recalled Item: FujiFilm FDR AQRO (Model DR-XD1000)- A digital mobile X-ray system Recalled...

The Issue: Arm which holds the tube head in place is susceptible to breaking, if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2023· Tobii Dynavox Llc

Recalled Item: Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device...

The Issue: Problem maintaining the stable placement of the battery may come loose from...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2023· Iradimed Corporation

Recalled Item: Iradimed Corporation MRidium MRI 1000 Series Infusion Sets Recalled by...

The Issue: Certain Iradimed 1057 Syringe Adapter Sets, used with the MRidium MRI...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2023· Aesculap Implant Systems LLC

Recalled Item: Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only and Recalled by...

The Issue: Mislabeled: Product is marked with GTIN # 04046955299592 however; the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2023· Olympus Corporation of the Americas

Recalled Item: Single Use Rotatable Clip Fixing Device Model HX 201LR 135 - Rotatable...

The Issue: There have been complaints that the clip did not come out of the tube sheath...

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

Class II — Potential Health HazardOngoing