Product Recalls in Hawaii

Product recalls affecting Hawaii — including food, drugs, consumer products, medical devices, and vehicles distributed to Hawaii. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 961 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
961 in last 12 months

Showing 35421–35440 of 47,764 recalls

Medical DeviceJuly 30, 2015· Beckman Coulter Inc.

Recalled Item: AU680 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
DrugJuly 29, 2015· Wockhardt Usa Inc.

Recalled Item: Lisinopril Tablets USP Recalled by Wockhardt Usa Inc. Due to CGMP...

The Issue: CGMP Deviations: An FDA inspection identified inadequate investigations of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2015· Wockhardt Usa Inc.

Recalled Item: Lisinopril Tablets USP Recalled by Wockhardt Usa Inc. Due to CGMP...

The Issue: CGMP Deviations: An FDA inspection identified inadequate investigations of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2015· Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals

Recalled Item: Lisinopril Tablets Recalled by Vintage Pharmaceuticals LLC dba Qualitest...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
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: 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: KimVent* Turbo-Cleaning 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: 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
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: 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 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* 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: KimVent* Turbo-Cleaning 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: 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* 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* Turbo-Cleaning 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