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 17411760 of 27,456 recalls

Medical DeviceApril 21, 2025· Capnia Inc

Recalled Item: Precision Sampling Set Recalled by Capnia Inc Due to Sampling set nasal...

The Issue: Sampling set nasal cannula used with End-Tidal Carbon Monoxide (ETCO)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2025· American Contract Systems, Inc.

Recalled Item: LOWER EXTREMITY Recalled by American Contract Systems, Inc. Due to Test...

The Issue: Test results for cast padding component included in procedure trays shows...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN...

The Issue: Due to a manufacturing defect IV catheter may have a hole in the septum,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2025· C.R. Bard Inc

Recalled Item: Bard¿ Single Intragastric Linton Balloon Tube Recalled by C.R. Bard Inc Due...

The Issue: Due to customer complaints, there is a potential for users to be unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2025· Cook Incorporated

Recalled Item: Check=Flo Performer Introducer Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2025· Cook Incorporated

Recalled Item: Check=Flo Performer Introducer Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2025· C.R. Bard Inc

Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate) Recalled by C.R....

The Issue: Due to customer complaints, there is a potential for users to be unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2025· C.R. Bard Inc

Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) Recalled by C.R. Bard...

The Issue: Due to customer complaints, there is a potential for users to be unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2025· C.R. Bard Inc

Recalled Item: Bard Minnesota Four Lumen Esophagogastric Tamponade Tube Recalled by C.R....

The Issue: Due to customer complaints, there is a potential for users to be unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2025· C.R. Bard Inc

Recalled Item: Bard Blakemore Esophageal-Nasogastric Tube (Adult) Recalled by C.R. Bard Inc...

The Issue: Due to customer complaints, there is a potential for users to be unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2025· Straumann USA LLC

Recalled Item: WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments....

The Issue: Incorrect blister labelling.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2025· Luminex Corporation

Recalled Item: VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test Recalled by...

The Issue: It was determined that the consumable issue may result in No Call - INT CTL...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2025· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus Pro Patient Monitor Recalled by Remote Diagnostic Technologies Ltd....

The Issue: software issue that causes an error screen on a portable vital signs monitor...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Homocysteine Calibrator (2 Pack). Siemens Material Number:...

The Issue: Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur HCY Calibrator (2 Pack). Siemens Material Number: 10310376....

The Issue: Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2025· Remote Diagnostic Technologies Ltd.

Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...

The Issue: Patient Monitor software update to address issues:1)May freeze at startup...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2025· Prismatik Dentalcraft, Inc.

Recalled Item: Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " Recalled by Prismatik...

The Issue: Due to packaging mix up. Package of finished devices were reported to have...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products CRP Slides. One sales unit contains 5 cartridges...

The Issue: Product was incorrectly assigned GEN 88 instead of GEN 83 on product carton,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2025· Straumann USA LLC

Recalled Item: Plus Initial Drill Recalled by Straumann USA LLC Due to The batch was...

The Issue: The batch was produced without the laser engraving of 7 mm.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2025· Augmedics Ltd.

Recalled Item: Augmedics Perc Pin Adaptor Recalled by Augmedics Ltd. Due to The perc pin...

The Issue: The perc pin adaptor AMCH07200 tightening knob was found to be inconvenient...

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

Class II — Potential Health HazardOngoing