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. 2,356 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,356 in last 12 months

Showing 3396133980 of 47,764 recalls

Medical DeviceDecember 16, 2015· Stryker Spine

Recalled Item: AccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF Recalled by Stryker...

The Issue: There were two potential interference conditions identified with the way the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A Recalled...

The Issue: An issue with the Panorama Central Station may cause the system to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: Anesthesia device service kits. ASSY-MSN Recalled by GE Medical Systems, LLC...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Bio-Rad Laboratories, Inc.

Recalled Item: D-10 Rack Loader Recalled by Bio-Rad Laboratories, Inc. Due to On a rare...

The Issue: On a rare occasion, there is a potential to assign a patient result to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and...

The Issue: The door latch may not fully close and the door may open unexpectedly. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: SlimeX-15 Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: Asset BOLD Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: Prime Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Baxter Healthcare Corp.

Recalled Item: Dextrose Injection Recalled by Baxter Healthcare Corp. Due to Presence of...

The Issue: Presence of Particulate Matter: Confirmed customer compliants of finding an...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: La' Trim Plus Capsules Recalled by Bee Extremely Amazed LLC Due to...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: Oasis Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: ZI XIU TANG BEAUTY FACE & FIGURE Capsules Recalled by Bee Extremely Amazed...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: SLIM TRIM U Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: EVOLVE BEE POLLEN Capsules Recalled by Bee Extremely Amazed LLC Due to...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: XCEL Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared Fluoxetine

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund