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. 2,338 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,338 in last 12 months

Showing 3748137500 of 47,764 recalls

DrugFebruary 12, 2015· Actavis Inc

Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2015· Par Pharmaceutical Inc.

Recalled Item: Mafenide Acetate Recalled by Par Pharmaceutical Inc. Due to Presence of...

The Issue: Presence of Foreign Substance; oxidized steel, organic material and shredded...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 12, 2015· Ameda, Inc.

Recalled Item: Ameda Dual Short Term HygieniKit Milk Collections System (SKU 17115)...

The Issue: Devices were not sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2015· Ameda, Inc.

Recalled Item: Ameda One-Hand Manual Breast Pump (SKU 17161) - Primary packaging Recalled...

The Issue: Devices were not sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Triathlon Distal Capture Assembly Catalog No: 6541-1-723 The Triathlon...

The Issue: Potential for weld disassociation of the cross pin, which could lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2015· Dako North America Inc.

Recalled Item: Autostainer Link 48 (AS480) Recalled by Dako North America Inc. Due to A...

The Issue: A false negative result affecting the diagnosis may occur. A defect in the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 11, 2015· Mylan Institutional LLC

Recalled Item: DOXOrubicin Hydrochloride Injection Recalled by Mylan Institutional LLC Due...

The Issue: Correct Labeled Product Mispack: Ifosfamide Injection 50 mg/mL, 60 mL,...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 11, 2015· Sunfood Corportation

Recalled Item: Organic Sacha Inchi Powder Recalled by Sunfood Corportation Due to Sunfood...

The Issue: Sunfood is recalling Sacha Inchi Powder because it has the potential to be...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 11, 2015· Sybron Dental Specialties

Recalled Item: Outer cardboard box labeling: Pinnacle Cure Sleeve Recalled by Sybron Dental...

The Issue: Cases of Cure Sleeve labeled with part number 4513, which fits 13mm tips,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· DePuy Orthopaedics, Inc.

Recalled Item: SMARTSET GHV Gentamicin Bone Cement. A self-curing Recalled by DePuy...

The Issue: One lot of SMARTSET GHV Gentamicin Bone Cement is partially agglomerated ....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Intuitive Surgical, Inc.

Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Intuitive Surgical has identified the potential for a certain, small portion...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Intuitive Surgical, Inc.

Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Intuitive Surgical has identified the potential for a certain, small portion...

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

Class II — Potential Health HazardOngoing
DrugFebruary 10, 2015· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Sulfate Extended-Release Capsules Recalled by Actavis...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 10, 2015· Tosoh Bioscience, Inc.

Recalled Item: G7 Variant Elution Buffer HiS no. 1 (M) component of Recalled by Tosoh...

The Issue: The G7 Variant Elution Buffer HiS no. 1 (M) is incorrectly labeled with an...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 9, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare DigitalDiagnost System X-Ray Recalled by Philips Medical...

The Issue: The system is designed to emit a beep upon termination of an exposure....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare DuraDiagnost X- Ray Recalled by Philips Medical Systems,...

The Issue: The system is designed to emit a beep upon termination of an exposure....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2015· CooperSurgical, Inc.

Recalled Item: CooperSurgical PESSARY KIT-CUBE#2 Recalled by CooperSurgical, Inc. Due to...

The Issue: Incorrect size printed on the Milex Pessary Kit packaging label

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

Class II — Potential Health HazardOngoing
DrugFebruary 6, 2015· Tarmac Products, Inc.

Recalled Item: Antacid Liquid Regular Strength Antacid & Anti-Gas (Aluminum hydroxide 200...

The Issue: Microbial Contamination of Non-Sterile Products: Lots failed microbiological...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 6, 2015· See's Candies Inc.

Recalled Item: See's Candies Classic Red Heart with Assorted Chocolates (8 oz. 227 g)...

The Issue: One packaging run of 8 oz. Classic Red Hearts with Assorted Chocolates was...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 6, 2015· Mars Food US

Recalled Item: UNCLE BEN'S(R) Ready Rice(R) NEW ORLEANS STYLE RED BEANS & RICE Recalled by...

The Issue: UNCLE BENS(R) Ready to Heat Pouches have the potential for containing metal...

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

Class II — Potential Health HazardOngoing
Refund