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. 2,363 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,363 in last 12 months

Showing 2474124760 of 47,970 recalls

Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature sensing catheter 14FR Recalled by Degania Silicone, Ltd. Due to...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Thermistor Foley catheter Recalled by Degania Silicone, Ltd. Due to The...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur CB Resolve Recalled by Ossur Americas Due to Halo system products...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur OB Resolve Recalled by Ossur Americas Due to Halo system products...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Skull Pin Recalled by Ossur Americas Due to Halo system products...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2018· Espiner Medical Ltd

Recalled Item: Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml...

The Issue: Label was incorrect. The label states that the volume of the retrieval bag...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2018· Boston Scientific Corporation

Recalled Item: Boston Scientific Maestro 4000 Cardiac Ablation System Recalled by Boston...

The Issue: Reports of unintended continuation of radiofrequency (RF) energy delivery...

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

Class II — Potential Health HazardOngoing
DrugJune 20, 2018· Gaia Ethnobotanical LLC

Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...

The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJune 20, 2018· Gaia Ethnobotanical LLC

Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...

The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJune 20, 2018· Gaia Ethnobotanical LLC

Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...

The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJune 20, 2018· Gaia Ethnobotanical LLC

Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...

The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJune 20, 2018· Gaia Ethnobotanical LLC

Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...

The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJune 20, 2018· Gaia Ethnobotanical LLC

Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...

The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJune 20, 2018· Gaia Ethnobotanical LLC

Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...

The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJune 20, 2018· Gaia Ethnobotanical LLC

Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...

The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund