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. 2,375 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,375 in last 12 months

Showing 2920129220 of 47,764 recalls

Medical DeviceMarch 28, 2017· Aesculap Implant Systems LLC

Recalled Item: GE426R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...

The Issue: Diamond particulates may break off the burr and fall into the surgical site....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Aesculap Implant Systems LLC

Recalled Item: GP321R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...

The Issue: Diamond particulates may break off the burr and fall into the surgical site....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Aesculap Implant Systems LLC

Recalled Item: GP161R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...

The Issue: Diamond particulates may break off the burr and fall into the surgical site....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Bard Peripheral Vascular Inc

Recalled Item: MR GHIATAS Beaded Breast Localization Wire Recalled by Bard Peripheral...

The Issue: It may be at risk of containing a non-MR compatible GHIATAS Beaded Breast...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Draegar Medical Systems, Inc.

Recalled Item: Kappa Recalled by Draegar Medical Systems, Inc. Due to It was reported that...

The Issue: It was reported that a set low O2 alarm does not go off although the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Draegar Medical Systems, Inc.

Recalled Item: Delta XL Recalled by Draegar Medical Systems, Inc. Due to It was reported...

The Issue: It was reported that a set low O2 alarm does not go off although the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Draegar Medical Systems, Inc.

Recalled Item: Delta Recalled by Draegar Medical Systems, Inc. Due to It was reported that...

The Issue: It was reported that a set low O2 alarm does not go off although the...

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

Class II — Potential Health HazardOngoing
DrugMarch 28, 2017· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Nystatin and Triamcinolone Acetonide Cream Recalled by Taro Pharmaceuticals...

The Issue: Failed Content Uniformity Specifications; out-of-specification (OOS) results...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 28, 2017· Teva Pharmaceuticals USA

Recalled Item: PrednisoLONE Oral Solution USP Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Stability Specifications

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

Class III — Low RiskOngoing
Refund
DrugMarch 28, 2017· Envy Me

Recalled Item: LaBri's Body Health Atomic Recalled by Envy Me Due to Undeclared Sibutramine

The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared Sibutramine.

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2017· Gary Wood

Recalled Item: hCG Body Shaper Recalled by Gary Wood Due to Marketed without an Approved...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis has found the product to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 27, 2017· Alcon Research, Ltd.

Recalled Item: Alcon Patient Care Kits Product Usage: A Patient Care Kit Recalled by Alcon...

The Issue: Alcon is initiating a Voluntary Medical Device Removal because the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Dale Medical Products, Inc.

Recalled Item: Dale Medical Stabilock Endotracheal Adhesive Base Product # 273 The Recalled...

The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Remel Inc

Recalled Item: Blood Agar (TSA w/ 5% Sheep Blood) Plate Recalled by Remel Inc Due to...

The Issue: Confirmed complaint of surface contamination of Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Dale Medical Products, Inc.

Recalled Item: Dale Medical Stabilock Endotracheal Tube Holder Product # 270 The Recalled...

The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Craftmatic Industries, Inc.

Recalled Item: Legacy Base for Dual Bed Configurations Recalled by Craftmatic Industries,...

The Issue: A potential for dual-configured beds to separate or slip away from one another.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Craftmatic Industries, Inc.

Recalled Item: Craftmatic Model 1 Base for Dual Bed Configurations Recalled by Craftmatic...

The Issue: A potential for dual-configured beds to separate or slip away from one another.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2017· Sysmex America Inc

Recalled Item: Sysmex Recalled by Sysmex America Inc Due to Reported customer complaints of...

The Issue: Reported customer complaints of automated hematology analyzers catching fire...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2017· Toshiba American Medical Systems

Recalled Item: Toshiba Medical Radrex - i Digital Radiography X-ray system Radrex-i...

The Issue: It was discovered during a procedure that when the operator made an exposure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2017· Merit Medical Systems, Inc.

Recalled Item: 1 mL Medallion¿ Syringe. Catalog Numbers: 701989001 Recalled by Merit...

The Issue: Merit Medical Systems announces a voluntary field action for the 1mL...

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

Class II — Potential Health HazardOngoing