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. 2,540 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,540 in last 12 months

Showing 1022110240 of 47,764 recalls

Medical DeviceNovember 23, 2022· Baxter Healthcare Corporation

Recalled Item: Revaclear 400 dialyzers. Indicated for treatment of chronic and acute...

The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...

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

Class II — Potential Health HazardOngoing
DrugNovember 22, 2022· Fresenius Kabi USA, LLC

Recalled Item: Sensorcaine (Bupivacaine HCl and Epinephrine Injection Recalled by Fresenius...

The Issue: Subpotent Drug: Testing results below the defined limit for the epinephrine...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 22, 2022· Fresenius Kabi USA, LLC

Recalled Item: Sensorcaine-MPF (Bupivacaine HCl and Epinephrine Injection Recalled by...

The Issue: Subpotent Drug: Testing results below the defined limit for the epinephrine...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 22, 2022· Fresenius Kabi USA, LLC

Recalled Item: Sensorcaine (Bupivacaine HCl and Epinephrine Injection Recalled by Fresenius...

The Issue: Subpotent Drug: Testing results below the defined limit for the epinephrine...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 22, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Fresenius Medical Care Holdings,...

The Issue: Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 22, 2022· Randox Laboratories Ltd.

Recalled Item: Liquid Assayed Specific Protein Control Level 2- In vitro diagnostic use...

The Issue: Concentration of Rheumatoid Factor has decreased in Specific Protein Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Randox Laboratories Ltd.

Recalled Item: Liquid Assayed Specific Protein- In vitro diagnostic use Recalled by Randox...

The Issue: Concentration of Rheumatoid Factor has decreased in Specific Protein Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Randox Laboratories Ltd.

Recalled Item: Liquid Assayed Specific Protein Control Level 3- In vitro diagnostic use...

The Issue: Concentration of Rheumatoid Factor has decreased in Specific Protein Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Philips North America Llc

Recalled Item: Philips SmartPath to Ingenia Elition X MR System Recalled by Philips North...

The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Philips North America Llc

Recalled Item: Philips MR 7700 System Recalled by Philips North America Llc Due to Gradient...

The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Philips North America Llc

Recalled Item: Philips Ingenia Elition S MR System Recalled by Philips North America Llc...

The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Philips North America Llc

Recalled Item: Philips Ingenia Elition X MR System Recalled by Philips North America Llc...

The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Philips North America Llc

Recalled Item: Philips Upgrade to MR 7700 System Recalled by Philips North America Llc Due...

The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...

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

Class II — Potential Health HazardOngoing
DrugNovember 21, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy Relief D Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 21, 2022· Philips North America Llc

Recalled Item: Philips Fetal Spiral Electrode-intended for patients requiring fetal heart...

The Issue: Fetal Spiral Electrode (FSE) spiral tip of the FSE breaking off during use...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2022· Becton Dickinson & Co.

Recalled Item: BBL Chocolate II Agar- IVD for the isolation and cultivation Recalled by...

The Issue: Boxes contain a reduced concentration of Nicotinamide Adenine Dinucleotide...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2022· Leica Microsystems, Inc.

Recalled Item: Leica MICROSYSTEMS M530 OHX Recalled by Leica Microsystems, Inc. Due to...

The Issue: There is a potential issue resulting in the Power Supply potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2022· Leica Microsystems, Inc.

Recalled Item: Leica MICROSYSTEMS Provido Recalled by Leica Microsystems, Inc. Due to There...

The Issue: There is a potential issue resulting in the Power Supply potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2022· Leica Microsystems, Inc.

Recalled Item: Leica MICROSYSTEMS Proveo 8 Recalled by Leica Microsystems, Inc. Due to...

The Issue: There is a potential issue resulting in the Power Supply potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2022· BioReference Health, LLC

Recalled Item: The 4Kscore Test is an in vitro serum or plasma Recalled by BioReference...

The Issue: SPM software anomalies that may lead to the generation of erroneous 4Kscore...

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

Class II — Potential Health HazardOngoing