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. 1,737 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
1,737 in last 12 months

Showing 4078140800 of 47,970 recalls

Medical DeviceApril 25, 2014· CryoLife, Inc.

Recalled Item: BG3515-5 US 5mL BioGlue Surgical Adhesive. BioGlue Surgical Adhesive...

The Issue: Serum albumin component monomer failed to meet internally established end of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· Hitachi Medical Systems America Inc

Recalled Item: Oasis Coil Extension Cable used with Hitachi Oasis MRI System Recalled by...

The Issue: The firm received a complaint stating the Coil Extension Cable accessory...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation software version 4.0.3.4 RayStation is a software system designed...

The Issue: This notice concerns a problem with the computation of ROI voxel volumes for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius 2008T Hemodialysis Machine with Revision K Actuator Test Boards...

The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Revision K Actuator Test Boards sold as replacement parts for Recalled by...

The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...

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

Class II — Potential Health HazardOngoing
DrugApril 25, 2014· Prestige Brands Holdings

Recalled Item: PediaCare brand NIGHTTIME MULTI-SYMPTOM Cold Recalled by Prestige Brands...

The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...

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

Class III — Low RiskOngoing
Refund
DrugApril 25, 2014· Prestige Brands Holdings

Recalled Item: PediaCare brand DAY & NIGHT Value Pack DAYTIME MULTI-SYMPTOM Cold Recalled...

The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...

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

Class III — Low RiskOngoing
Refund
DrugApril 24, 2014· Baxter Healthcare Corp.

Recalled Item: Famotidine Injection 20 mg Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter: Baxter Healthcare Corporation has received a...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2014· Actavis Laboratories, FL, Inc.

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Recall due to complaints of split or...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2014· Actavis Laboratories, FL, Inc.

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Recall due to complaints of split or...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 8"x10" Reorder Number: Recalled by...

The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Mar Cor Purification

Recalled Item: Mar Cor Purification Recalled by Mar Cor Purification Due to Mar Cor...

The Issue: Mar Cor Purification manufactured Central Water Plant (CWP) reverse osmosis...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: DISP 9730951 STRL SPHERE Recalled by Medtronic Navigation, Inc. Due to...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: PACK 9731975 TUMOR RESECTION AXIEM CR Recalled by Medtronic Navigation, Inc....

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: BAG 9732315 MOUSE STERILE 15 PK Recalled by Medtronic Navigation, Inc. Due...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: PIN Recalled by Medtronic Navigation, Inc. Due to Medtronic Navigation is...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: PATIENT TRACKER 9733534XOM ENT 1PK Recalled by Medtronic Navigation, Inc....

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: PAK 9733497 NAV NIM-SPINE PEDICLE ACC KT Recalled by Medtronic Navigation,...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: BIOPSY NEEDLE KIT Recalled by Medtronic Navigation, Inc. Due to Medtronic...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: INST 9731132 KIT CR DRIVER 5PK Recalled by Medtronic Navigation, Inc. Due to...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

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

Class II — Potential Health HazardOngoing