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. 2,556 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,556 in last 12 months

Showing 54615480 of 47,764 recalls

Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with Luer Slip Tips labeled as: 1) SOL-M 1ml Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with Low Dead Space labeled as: a) SOL-M 1ml Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with exchangeable needles labeled as: SOL-CARE: 1) SOL-CARE 10ml...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with Fixed Needles labeled as: a) SOL-M: 1) SOL-M Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringe Tip Caps labeled as: 1) SOL-M Syringe Tip Cap Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Echonous Inc

Recalled Item: Kosmos on iOS impacting iOS Recalled by Echonous Inc Due to Ultrasound...

The Issue: Ultrasound system has a bug in affected iOS software, which after DICOM...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· First Source Inc

Recalled Item: First Source Vision M. Portable cart and platform that supports Recalled by...

The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· First Source Inc

Recalled Item: First Source iQ Flex M. Portable cart and platform that Recalled by First...

The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Stryker GmbH

Recalled Item: Stryker Hoffman LRF Wire Tensioner Recalled by Stryker GmbH Due to The...

The Issue: The adjustment ring on the device may become loose resulting in the wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· C.R. Bard Inc

Recalled Item: Bard Medical SureStep Foley Tray System Recalled by C.R. Bard Inc Due to...

The Issue: Some of the devices may function incorrectly resulting in no temperature...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Remote Diagnostic Technologies Ltd.

Recalled Item: Philips Tempus LS-Manual Defibrillator Recalled by Remote Diagnostic...

The Issue: Simultaneous ECG measurements with multiple devices, including a manual...

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

Class II — Potential Health HazardOngoing
DrugMay 8, 2024· Lupin Pharmaceuticals Inc.

Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: Defective container: lack of seal integrity.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 8, 2024· Baxter Healthcare Corporation

Recalled Item: Centrella Max - The Centrella Smart+ Bed is intended for Recalled by Baxter...

The Issue: There is a potential for the top cover of the hospital bed mattress to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2024· Thoratec Corp.

Recalled Item: Thoratec HeartMate System Monitor Recalled by Thoratec Corp. Due to System...

The Issue: System monitor screen may display atypical behavior: Overlapping...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 8, 2024· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient...

The Issue: Reports of patient burns.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 8, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Range Verifier - In vitro...

The Issue: The results generated by the VITROS Immunodiagnostic Products Vitamin B12...

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

Class III — Low RiskOngoing
DrugMay 7, 2024· PACIRA PHARMACEUTICALS INC

Recalled Item: Drug Vial Label: Zilretta¿ (triamcinolone acetonide extended-release...

The Issue: Failed Stability Specifications - at 12 months 2-8 degrees C followed by 6...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 7, 2024· MACLEODS PHARMA USA, INC

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by MACLEODS...

The Issue: Presence of foreign substance: plastic-like substance.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 7, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider...

The Issue: Potential for an incomplete seal on the packaging tray.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Blunt Tip Recalled by MEDLINE...

The Issue: Potential for an incomplete seal on the packaging tray.

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

Class II — Potential Health HazardOngoing