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 2216122180 of 47,764 recalls

Medical DeviceFebruary 14, 2019· ACell, Inc

Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...

The Issue: The devices were released from a lot for which one sample failed to meet the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· ACell, Inc

Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...

The Issue: The devices were released from a lot for which one sample failed to meet the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 13, 2019· Perrigo New York, Inc.

Recalled Item: Ciclopirox shampoo 1% Recalled by Perrigo New York, Inc. Due to Failed...

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

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

Class III — Low RiskOngoing
Refund
DrugFebruary 13, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Lovastatin Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: Finished product made with lovastatin drug substance that...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery Ml DR Product Usage: The systems are intended for Recalled by GE...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery Ml Product Usage: The systems are intended for head Recalled by GE...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery PET/CT 610 Product Usage: The systems are intended for Recalled by...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Optima PET/CT 560 Recalled by GE Healthcare, LLC Due to GE Healthcare PET/CT...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery PET/CT 710 Product Usage: The systems are intended for Recalled by...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery IQ Product Usage: The systems are intended for head Recalled by GE...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2019· Smiths Medical ASD Inc.

Recalled Item: Portex Blue Line Ultra Tracheostomy Tube Inner Cannula. One cannula Recalled...

The Issue: Packaged with an incorrect size inner cannula.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2019· Smiths Medical ASD Inc.

Recalled Item: Smith Medical JELCO Hypodermic Needle-Pro EDGE Safety Device Safety Device...

The Issue: Incorrect needle length and gage.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2019· Fenwal Inc

Recalled Item: Vacuum Unit for CATSmart Vacuum Pump. Fresenius CATSmart (Continuous...

The Issue: The optional Vacuum Unit may stop working and display the failure message...

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

Class II — Potential Health HazardOngoing
DrugFebruary 8, 2019· McDaniel Life-Line LLC

Recalled Item: Indian Herb Paste (a dietary supplement) Ingredients: Galangal Recalled by...

The Issue: Unapproved new drug

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 8, 2019· McDaniel Life-Line LLC

Recalled Item: Life-Line tm Catalytic Activated Energy Water Recalled by McDaniel Life-Line...

The Issue: Unapproved new drug

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 8, 2019· World Waters, LLC dba WTRMLN WTR

Recalled Item: Watermelon Recalled by World Waters, LLC dba WTRMLN WTR Due to Cold Pressed...

The Issue: Cold Pressed Juice Watermelon WTRMLN WTR Original 12 packs due to the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 8, 2019· Canon Medical System, USA, INC.

Recalled Item: Infinix DP- i(Infinix-8000F) CAT-870B Catheterization Table (Titling) -...

The Issue: Table tilts without operator involvement as a result of liquid spilling into...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Cardiohelp Emergency Drive Recalled by Maquet Cardiovascular Us Sales, Llc...

The Issue: Upon servicing the gearwheel in the Emergency Drive the gearwheel may have...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 8, 2019· Draegar Medical Systems, Inc.

Recalled Item: Infinity Delta Family patient monitors The Infinity Delta Series...

The Issue: The firm is recalling their Delta family of patient monitors software due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Draegar Medical Systems, Inc.

Recalled Item: Omega Systems These devices are intended to be used in Recalled by Draegar...

The Issue: The firm is recalling their Delta family of patient monitors software due to...

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

Class II — Potential Health HazardOngoing