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. 2,350 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,350 in last 12 months

Showing 3548135500 of 47,764 recalls

DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: CVS Pharmacy Recalled by Ohm Laboratories, Inc. Due to Superpotent Drug: Out...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Up&Up loratadine orally disintegrating tablets Recalled by Ohm Laboratories,...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Good Neighbor Pharmacy Loratadine Orally Disintegrating Tablets Recalled by...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 27, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for z-statistic related to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 27, 2015· Advanced Sterilization Products

Recalled Item: CIDEX Activated Dialdehyde Solution Recalled by Advanced Sterilization...

The Issue: Advanced Sterilization Products (ASP) is recalling the CIDEX Activated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...

The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Sunrise Medical (US) LLC

Recalled Item: Zippie IRIS Wheelchair. model EIZ5A in combination with option code Recalled...

The Issue: Quickie IRIS and Zippie IRIS tilt-in-space wheelchairs with MONO Backrest...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...

The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Leica Microsystems, Inc.

Recalled Item: The Leica ASP6025 Tissue Processor. Pathology and Hematology Departments....

The Issue: The ASP6025 Tissue Processor instrument is incorrectly getting into a state...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ Folate Ascorbic Acid/Ascorbic Acid Diluent Recalled by...

The Issue: Low red blood cell control recoveries and low results for red blood cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...

The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...

The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...

The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Sunrise Medical (US) LLC

Recalled Item: Quickie IRIS Wheelchair. model EIZ4-2 in combination with option code...

The Issue: Quickie IRIS and Zippie IRIS tilt-in-space wheelchairs with MONO Backrest...

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

Class II — Potential Health HazardOngoing