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. 2,269 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,269 in last 12 months

Showing 4370143720 of 47,970 recalls

Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 65597201131 Femur CR POR FEM SURF HDN HATCP AML Rx Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597001131 Femur CR PRC SURF HDN FEM CO-NID AML Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 90595203117 Articular Surface XLPE CR ART SURF AE34/STYEL 17 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Codman & Shurtleff, Inc.

Recalled Item: MedStream Programmable Infusion Pump- Implantable for the intrathecal...

The Issue: Miscalibrated Fill Level Sensor may affect dosing level

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 7, 2013· Codman & Shurtleff, Inc.

Recalled Item: MedStream Programmable Infusion Pump Recalled by Codman & Shurtleff, Inc....

The Issue: Miscalibrated Fill Level Sensor may affect dosing level

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 7, 2013· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Sets The Paradigm infusion sets...

The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Medtronic is recalling...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Intermate Infusion Pump. Indicated for the intravenous...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Regional Analgesia Infusor System with Patient Control....

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Intermate Infusion Pump. Indicated for the intravenous...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Coiled Tube Infusors (Portable Elastomeric Infusion Systems)....

The Issue: Due to an increase in complaints for leaks at the distal male Luer and Luer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: SV Elastomeric Infusion Device. Indicated for the intravenous...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Multirate Infusor Devices. Indicated for the intravenous...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Infusor SV and LV Elastomeric Infusion Devices. Indicated...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Multiday lnfusor Recalled by Baxter Healthcare Corp. Due to Due...

The Issue: Due to an increase in complaints for leaks at the distal male Luer and Luer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Basal/Bolus Infusor. Indicated for the intravenous...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
DrugJune 6, 2013· Novartis Consumer Health

Recalled Item: Excedrin Migraine (Acetaminophen 250 mg Recalled by Novartis Consumer Health...

The Issue: Defective container: products are packaged in pouches which may not have...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2013· Novartis Consumer Health

Recalled Item: Parsel Plus ( US product: Excedrin Tension Headache) (Acetaminophen 500...

The Issue: Defective container: products are packaged in pouches which may not have...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2013· Novartis Consumer Health

Recalled Item: No Doz Recalled by Novartis Consumer Health Due to Defective container:...

The Issue: Defective container: products are packaged in pouches which may not have...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2013· Novartis Consumer Health

Recalled Item: Excedrin Extra Strength (Acetaminophen 250 mg Recalled by Novartis Consumer...

The Issue: Defective container: products are packaged in pouches which may not have...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2013· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The product has the potential for solution...

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

Class II — Potential Health HazardOngoing
Refund