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. 2,322 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,322 in last 12 months

Showing 3986139880 of 47,764 recalls

DrugJune 24, 2014· Doctor's Best, Inc.

Recalled Item: Doctor's Best Red Yeast Rice 1200 Recalled by Doctor's Best, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis discovered undeclared...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 24, 2014· Bard Access Systems

Recalled Item: Bard Peripherally Inserted Central Catheter (PICC) and Dialysis catheter...

The Issue: Potential for inadvertent scalpel stick injury involving the safety scalpel.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Surgical System Console Recalled by Stryker Instruments...

The Issue: The firm received complaints regarding insufficient irrigation to the tip of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2014· Invacare Corporation

Recalled Item: MK5 NX Controller--Wheelchair controller Recalled by Invacare Corporation...

The Issue: M41 Powered Wheelchairs received through Invacare Service Parts (ISP) have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...

The Issue: Complaints of failed calibration.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...

The Issue: Complaints of failed calibration.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT: product code 882482 Recalled by Philips Medical Systems...

The Issue: Flat Panel Display (FPD) failed to remain securely locked in the deployed...

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

Class II — Potential Health HazardOngoing
DrugJune 20, 2014· Novel Laboratories, Inc.

Recalled Item: Famotidine for Oral Suspension Recalled by Novel Laboratories, Inc. Due to...

The Issue: Failed Impurity/Degradation Specification; 12-month stability time point

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

Class III — Low RiskOngoing
Refund
DrugJune 20, 2014· Mylan Pharmaceuticals Inc.

Recalled Item: Tolterodine Tartrate Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications; Out of specification for...

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

Class III — Low RiskOngoing
Refund
FoodJune 20, 2014· Modern Macaroni Co Ltd

Recalled Item: Hula Brand Products Recalled by Modern Macaroni Co Ltd Due to FDA sample...

The Issue: FDA sample 466576 found 208.46 ppm of Sulfites in Hana Ebi dried shrimp product.

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

Class III — Low RiskOngoing
Refund
FoodJune 20, 2014· Modern Macaroni Co Ltd

Recalled Item: Hula Brand Products Recalled by Modern Macaroni Co Ltd Due to FDA sample...

The Issue: FDA sample 466576 found 208.46 ppm of Sulfites in Hana Ebi dried shrimp product.

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 20, 2014· Stryker Endoscopy

Recalled Item: Disposable StrykeFlow Tip Recalled by Stryker Endoscopy Due to Internal...

The Issue: Internal review found that six lots of Disposable StrykeFlow Tips were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2014· Laser Peripherals LLC

Recalled Item: LP Recalled by Laser Peripherals LLC Due to Mislabeling

The Issue: Laser Peripherals LLC is recalling DBLF-60-2 Bare Laser due to a mislabeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2014· ORIGIO, Inc

Recalled Item: Name: Pasteur Pipets Recalled by ORIGIO, Inc Due to Identification of...

The Issue: Identification of packaging breach of the nylon pouch sterile barrier for...

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

Class II — Potential Health HazardOngoing
DrugJune 19, 2014· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended Release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

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

Class III — Low RiskOngoing
Refund
DrugJune 19, 2014· Mckesson Packaging Services

Recalled Item: Aspirin DR Enteric Coated Tablets Recalled by Mckesson Packaging Services...

The Issue: Failed Dissolution Specification; at the 12 month time interval.

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

Class III — Low RiskOngoing
Refund
DrugJune 19, 2014· Pfizer Inc.

Recalled Item: Cardura XL (doxazosin mesylate extended release tablets Recalled by Pfizer...

The Issue: Failed Impurities/Degradation Specifications: Product from this lot may not...

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

Class III — Low RiskOngoing
Refund
DrugJune 19, 2014· Forest Pharmaceuticals Inc

Recalled Item: Bystolic (nebivolol) tablets Recalled by Forest Pharmaceuticals Inc Due to...

The Issue: Failed Dissolution Specifications: Drug failed stage III dissolution testing.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 19, 2014· Country Life

Recalled Item: Country Life TARGET MINS CALCIUM MAGNESIUM With Vitamin D3 Complex Recalled...

The Issue: The affected lots do not meet quality standards due to insoluble particulates.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 19, 2014· Abbott Molecular

Recalled Item: 5 mL Reaction Vessels (a consumable of the Abbott m2000sp Recalled by Abbott...

The Issue: Abbott Molecular identified that some of the 5 ml Reaction Vessels (RVs)...

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

Class II — Potential Health HazardOngoing