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. 2,386 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,386 in last 12 months

Showing 2480124820 of 47,764 recalls

Medical DeviceMay 30, 2018· Baxter Healthcare Corporation

Recalled Item: FLOSEAL Special Applicator Tips in cartons labeled in part Recalled by...

The Issue: Baxter r recalled this device due to the use of an incorrect plastic...

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

Class II — Potential Health HazardOngoing
DrugMay 29, 2018· Pharmaceutical Associates Inc

Recalled Item: Nystatin Oral Suspension Recalled by Pharmaceutical Associates Inc Due to...

The Issue: Resuspension problems: Out of specification for appearance and resuspendability.

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 29, 2018· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Implant Direct Legacy Implant Closed-Tray Transfer-Concave Profile Recalled...

The Issue: Cap may be mislabeled with incorrect part number, although the correct part...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2018· Zeiss, Carl Inc

Recalled Item: Disinfection unit UV (432332-9020-000) for the Celldiscoverer 7 microscope...

The Issue: Under certain circumstances, the firmware makes it possible for the...

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

Class II — Potential Health HazardOngoing
DrugMay 25, 2018· Shadow Holdings DBA Bocchi Labs

Recalled Item: X-Jow (menthol USP) Pain Gel Recalled by Shadow Holdings DBA Bocchi Labs Due...

The Issue: CGMP Deviations: products may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2018· Shadow Holdings DBA Bocchi Labs

Recalled Item: Acne Shave 3 Step Shaving System Recalled by Shadow Holdings DBA Bocchi Labs...

The Issue: CGMP Deviations: products may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2018· Shadow Holdings DBA Bocchi Labs

Recalled Item: Acne Shave Post-Shave Moisturizer (salicylic acid) Recalled by Shadow...

The Issue: CGMP Deviations: products may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2018· Shadow Holdings DBA Bocchi Labs

Recalled Item: Acne Shave (salicylic acid) Shave Cream Acne Shield Recalled by Shadow...

The Issue: CGMP Deviations: products may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 25, 2018· Dean Foods, Inc.

Recalled Item: Baskin Robbins Mint Chocolate Chip Recalled by Dean Foods, Inc. Due to...

The Issue: Product may contain unlabeled coconut.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 25, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis with Laird Cooling Unit for SSFD: Material # Recalled by Siemens...

The Issue: Due to a defective sealing, coolant may inflow into the electrical parts of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee systems with Laird Cooling Unit for SSFD: Material Recalled by...

The Issue: Due to a defective sealing, coolant may inflow into the electrical parts of...

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

Class II — Potential Health HazardOngoing
DrugMay 24, 2018· Allergan, PLC.

Recalled Item: Allergan Taytulla Softgel Capsules Recalled by Allergan, PLC. Due to...

The Issue: Contraceptive Tablets Out of Sequence.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Sorting-Drive Product Part Recalled by Beckman Coulter Inc. Due to...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Intelligent Peri-Analytical Workstation (HW+SW) Recalled by Beckman Coulter...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Sorting-Drive Professional Part Recalled by Beckman Coulter Inc. Due to...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Optima CT 540 Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing