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. 2,480 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,480 in last 12 months

Showing 1458114600 of 27,645 recalls

Medical DeviceOctober 8, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS¿ Chemistry Products dLDL Reagent-GENs 26 & 27. In Vitro Recalled by...

The Issue: VITROS Chemistry Products dLDL Reagent GENs 26 and 27, negatively biased results

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2018· GE Healthcare, LLC

Recalled Item: GE HEALTHCARE CARESCAPE R860 Inspiratory Safety Guard Recalled by GE...

The Issue: The ventilator Inspiratory Safety Guard (ISG) may disconnect from the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 5, 2018· Tosoh Bioscience Inc

Recalled Item: Hemoglobin A1c Control Recalled by Tosoh Bioscience Inc Due to Tosoh...

The Issue: Tosoh Bioscience has become aware of potential degradation of HbA1c control...

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

Class III — Low RiskOngoing
Medical DeviceOctober 5, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-900 Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience...

The Issue: Tosoh Bioscience has become aware of a potential issue with the pickup arm...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2018· Covidien LLC

Recalled Item: Parietex Composite Parastomal Mesh (Product Number PCOPM15 / PCOPM20)...

The Issue: The firm is issuing this voluntary removal following receipt of reports of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-900 Automated Immunoassay Analyzer Recalled by Tosoh Bioscience Inc Due...

The Issue: Tosoh Bioscience has become aware of a potential issue with the axis base of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2018· Ohmeda Medical

Recalled Item: Giraffe Omnibed - Product Usage: The OmniBed is a combination Recalled by...

The Issue: GE Healthcare has become aware of a potential safety issue that can occur if...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2018· GE Medical Systems, LLC

Recalled Item: SIGNA Architect system Product Usage: The Signa Architect system is Recalled...

The Issue: A small area on the bore surface, which is normally accessible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2018· Medtronic Inc.

Recalled Item: Medtronic MiniMed 630G 6025805-003_C Recalled by Medtronic Inc. Due to...

The Issue: Reports of occurrences in which insulin pumps with version 4.10 software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF 550 x 8ML/HR 2ML 15LO CPNBMT8015XL CP Recalled by Arrow International Inc...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF w/AS 550 x 1-14ML/HR CPNB Recalled by Arrow International Inc Due to...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 Deg 9x165mm Recalled by Zimmer Biomet,...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF w/AS 550 x 1-14 ml/hr Recalled by Arrow International Inc Due to Possible...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 Deg 11x300mm Recalled by Zimmer Biomet,...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail 125 Deg 12x165mm Recalled by Zimmer Biomet, Inc....

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left Deg 9x300mm Recalled by Zimmer Biomet, Inc....

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 130 Deg 11x300mm Recalled by Zimmer Biomet,...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF w/AS 550 x 0.5-7 ml Recalled by Arrow International Inc Due to Possible...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: 0F 550 x 8ML/HR 2ML 60LO CPNB Recalled by Arrow International Inc Due to...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF550x5ML/H 2ML 60LO 6" DUAL CATHS Recalled by Arrow International Inc Due...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing