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. 2,391 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,391 in last 12 months

Showing 2310123120 of 47,764 recalls

DrugSeptember 17, 2018· Otsuka Pharmaceutical Development & Commercialization, Inc.

Recalled Item: treatNOW ABILIFY (aripiprazole) and ABILIFY MAINTENA (aripiprazole) 400MG...

The Issue: Labeling Not Elsewhere Classified: Physician sample kits/cartons of treatNOW...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 17, 2018· Endo Pharmaceuticals, Inc.

Recalled Item: robaxin-750 (methocarbamol tablets Recalled by Endo Pharmaceuticals, Inc....

The Issue: Labeling: Incorrect Instructions: Dosage information on the immediate...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 17, 2018· Medline Industries Inc

Recalled Item: SparkleFresh Fluoride Toothpaste Recalled by Medline Industries Inc Due to...

The Issue: Microbial Contamination of Non-Sterile Product

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Millennium MG Multi-Geometry Digital CSE Dual Detector Gamma...

The Issue: A detector can detach and fall.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 14, 2018· Luminex Corporation

Recalled Item: VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as...

The Issue: Potential to lead to a false negative results.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH...

The Issue: A detector can detach and fall.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Disposable Accessory Kit Recalled by Ecolab Inc Due to The pouches of...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE LOGIQ E10 Ultrasound System Recalled by GE Healthcare, LLC Due to There...

The Issue: There is a potential for an undetected over temperature condition on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Disposable Accessory Kit Recalled by Ecolab Inc Due to The pouches of...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Millennium MC Recalled by GE Healthcare, LLC Due to A detector...

The Issue: A detector can detach and fall.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Camera Arm Drape (Box of 20) individually sealed in poly-Tyvek Recalled by...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek Recalled...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo¿ Advanced Perfusion System 1 Electronic Patient Gas System Recalled...

The Issue: The service manual was not updated at the time of the release of software...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2018· Roche Diagnostics Corporation

Recalled Item: CoaguChek¿ XS System Prothrombin time test: CoaguChek XS PT Test 2X24 Strips...

The Issue: Abnormally high INR test results with the affected CoaguChek test strips

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

Class I — Serious Health HazardOngoing
FoodSeptember 13, 2018· Swanson Health Products, Inc

Recalled Item: Swanson Ultra Recalled by Swanson Health Products, Inc Due to Himalayan...

The Issue: Himalayan Crystal Salt may contain metal wire pieces.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 12, 2018· Sarap Asian Fusion

Recalled Item: Miso Milo Chocolate (cookies) Recalled by Sarap Asian Fusion Due to...

The Issue: Undeclared wheat and soy lecithin

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 12, 2018· Swire Coca Cola USA

Recalled Item: Caffeine-Free Barq s Root Beer 12 Pack Recalled by Swire Coca Cola USA Due...

The Issue: Recalling Caffeine-Free Barq s Root Beer 12 Pack due to mislabeling.

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

Class III — Low RiskOngoing
Refund
FoodSeptember 12, 2018· Sarap Asian Fusion

Recalled Item: Ube Cookies & Cream (cookies) Recalled by Sarap Asian Fusion Due to...

The Issue: Undeclared wheat, soy lecithin, and milk

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 12, 2018· Sarap Asian Fusion

Recalled Item: Black Sesame White Chocolate (cookies) Recalled by Sarap Asian Fusion Due to...

The Issue: Undeclared wheat, soy lecithin, and milk

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 12, 2018· Sarap Asian Fusion

Recalled Item: Matcha Chocolate (cookies) Recalled by Sarap Asian Fusion Due to Undeclared...

The Issue: Undeclared wheat and soy lecithin

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

Class II — Potential Health HazardOngoing
Refund