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 2822128240 of 47,970 recalls

Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Non-Rebreather Mask w 7 (2.1 m) No-Crush Tubing Recalled by ConvaTec, Inc...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Pediatric Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Rebreathing Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Non-Rebreather Oxygen Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Rebreather Oxygen Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Oxygen Masks Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Non-Rebreathing Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· Zimmer Biomet Spine Inc.

Recalled Item: Vitality Spinal Fixation System Recalled by Zimmer Biomet Spine Inc. Due to...

The Issue: Zimmer Biomet is conducting a medical device recall for Vitality T27 Final...

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

Class II — Potential Health HazardOngoing
DrugMay 9, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Montelukast Sodium Oral Granules Recalled by Mylan Pharmaceuticals Inc. Due...

The Issue: Failed Impurities/Degradation Specifications; out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugMay 9, 2017· Strides Pharma INC

Recalled Item: Benzonatate capsules Recalled by Strides Pharma INC Due to Failed Stability...

The Issue: Failed Stability Specifications: Out of Specification results obtained for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 9, 2017· Covidien LLC

Recalled Item: Covidien Endo Peanut 5mm Auto Suture Blunt Dissector Item Code: Recalled by...

The Issue: Cotton tip of the device may disengage due to insufficient adhesive

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: Arrow Pressure Injectable PICC Kit Catheter Recalled by Arrow International...

The Issue: The Arrow Pressure Injectable PICC is intended for short-term or long-term...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) Introducer Kit with Integral Hemostasis Valve/Side Port Recalled by Arrow...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: Arterial Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) Pressure Injectable Multi-Lumen Central Venous Catheterization Kit 2)...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Recalled...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R)...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit 2) Recalled by...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) ARROWg+ard Blue You-Blend Two-Lumen Hemodialysis Catheterization Kit for...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing