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. 2,376 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,376 in last 12 months

Showing 2212122140 of 47,970 recalls

Medical DeviceMarch 29, 2019· GE Healthcare, LLC

Recalled Item: Prestige II Recalled by GE Healthcare, LLC Due to There has been a reported...

The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· GE Healthcare, LLC

Recalled Item: Silhouette VR This fully integrated system offers intuitive controls with...

The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· GE Healthcare, LLC

Recalled Item: Proteus XR/a The Proteus XR/a radiographic system offers the flexibility...

The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· Conformis, Inc.

Recalled Item: Conformis iTotal Hip Replacement System: HBS-033-00xx-010101 Recalled by...

The Issue: Discrepancy of 3mm between the values displayed and approved by surgeons in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· Conformis, Inc.

Recalled Item: Conformis iTotal Hip Replacement System: HBS-033-00xx-020101 Recalled by...

The Issue: Discrepancy of 3mm between the values displayed and approved by surgeons in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· GE Healthcare, LLC

Recalled Item: Precision 500D The Precision 500D R&F X-ray System is intended Recalled by...

The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· Centurion Medical Products Corporation

Recalled Item: Sterile Nail Clipper Concave Edge (67710) Recalled by Centurion Medical...

The Issue: Compromised seal on the sterile barrier pouch.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· Centurion Medical Products Corporation

Recalled Item: Sterile Nail Nipper Recalled by Centurion Medical Products Corporation Due...

The Issue: Compromised seal on the sterile barrier pouch.

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

Class II — Potential Health HazardOngoing
FoodMarch 28, 2019· Iowa Corn Processors

Recalled Item: Yellow Corn Flour #600 Unenriched Recalled by Iowa Corn Processors Due to...

The Issue: Product could contain foreign objects (pliable blue plastic)

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 28, 2019· Iowa Corn Processors

Recalled Item: Yellow Corn Flour #620 Recalled by Iowa Corn Processors Due to Foreign...

The Issue: Product could contain foreign objects (pliable blue plastic)

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 28, 2019· Boston Salads & Provisions Co., Inc.

Recalled Item: Edamame Salad sold under the following labels: BOSTON SALADS Prepared...

The Issue: Possible metal fragment contamination.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Zimmer Biomet, Inc.

Recalled Item: T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Recalled...

The Issue: There is a potential of fracture, bending or shearing of the driver.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Zimmer Biomet, Inc.

Recalled Item: T7 Driver Solid AO (Part Number 110018541) Product Usage: The Recalled by...

The Issue: There is a potential of fracture, bending or shearing of the driver.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...

The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 28, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...

The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...

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

Class I — Serious Health HazardOngoing
FoodMarch 27, 2019· Theo Chocolate Inc

Recalled Item: Sea Salt 70% Dark Chocolate 3 oz. bars Recalled by Theo Chocolate Inc Due to...

The Issue: Theo Chocolate Sea Salt 70% Dark Chocolate Bar is recalled due to undeclared...

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

Class I — Serious Health HazardOngoing
Refund