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. 2,390 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,390 in last 12 months

Showing 2098121000 of 27,456 recalls

Medical DeviceJuly 30, 2015· Beckman Coulter Inc.

Recalled Item: AU5800 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman coulter has received complaints regarding leaking and cracked C...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2015· Arrow International Inc

Recalled Item: Arrow International Recalled by Arrow International Inc Due to saline...

The Issue: saline leakage from unsecured connections between the Touhy Borst adaptor...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2015· Beckman Coulter Inc.

Recalled Item: AU480 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman coulter has received complaints regarding leaking and cracked C...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction Systems for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Multi-Access Port Replacement Catheter for Adults Recalled by...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Multi-Access Port Closed Suction System for Adults Recalled by...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Synthes (USA) Products LLC

Recalled Item: VEPTR Vertical Expandable Prosthetic Titanium Rib Recalled by Synthes (USA)...

The Issue: The last hole on certain VEPTR Inferior Cradles may be partially formed....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Neonates/Pediatrics Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Neonates/Pediatrics Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Wet Pak* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Synthes (USA) Products LLC

Recalled Item: Synthes Trauma Ex-Fix System (Small Recalled by Synthes (USA) Products LLC...

The Issue: Labeling changes were made related to MR conditions that align with standard...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Synthes (USA) Products LLC

Recalled Item: Synthes Sciatic Nerve Retractor and Sciatic Nerve Retractor Long Recalled by...

The Issue: Potential for micropores to form, allowing fluid to enter the hollow handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing