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. 2,351 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,351 in last 12 months

Showing 2724127260 of 47,970 recalls

DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: NORepinephrine Bitartrate 8 mg in 0.9% Sodium Chloride 250 mL Recalled by...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: fentaNYL 10 mcg/mL PF in Sodium Chloride 250 mL (Total Dose=2500 mcg)...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: Potassium Chloride 40 meq Added to Sodium Chloride 0.9% 250 mL Recalled by...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 14, 2017· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: A-Series A3/A5 Anesthesia Delivery System Recalled by Mindray DS USA, Inc....

The Issue: A software issue may result in the previous settings being applied instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: A-Series A7 Anesthesia Delivery System Recalled by Mindray DS USA, Inc. dba...

The Issue: A software issue may result in the previous settings being applied instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Panoramic Rental Corp.

Recalled Item: PC-1000 Recalled by Panoramic Rental Corp. Due to The lift motor used to...

The Issue: The lift motor used to raise and lower the overhead chassis will wear if not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2017· Microline Surgical, Inc.

Recalled Item: The ReNew Reusable Grasper and Dissector Tips are to be Recalled by...

The Issue: The heat-shrink insulation tube may split during autoclave...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2017· Medtronic Vascular Galway DBA Medtronic Ireland

Recalled Item: Euphora Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...

The Issue: Stylette removal difficulties on the Euphora and Solarice products.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2017· Medtronic Vascular Galway DBA Medtronic Ireland

Recalled Item: Solarice Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...

The Issue: Stylette removal difficulties on the Euphora and Solarice products.

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

Class II — Potential Health HazardOngoing
DrugJuly 12, 2017· Akorn Inc

Recalled Item: Halyard 24-Hour Oral Care Kit q2 Recalled by Akorn Inc Due to...

The Issue: Crystallization with subpotent out of specification assay results for...

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

Class III — Low RiskOngoing
Refund
DrugJuly 12, 2017· Akorn Inc

Recalled Item: Chlorhexidine Gluconate Oral Rinse Recalled by Akorn Inc Due to...

The Issue: Crystallization with subpotent out of specification assay results for...

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

Class III — Low RiskOngoing
Refund
DrugJuly 12, 2017· Akorn Inc

Recalled Item: Halyard 24-Hour Oral Care Kit q4 Recalled by Akorn Inc Due to...

The Issue: Crystallization with subpotent out of specification assay results for...

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

Class III — Low RiskOngoing
Refund
DrugJuly 12, 2017· Pfizer Inc.

Recalled Item: Deferoxamine Mesylate for injection Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Firm failed to control impurity for color change at the API...

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

Class III — Low RiskOngoing
Refund