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. 968 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
968 in last 12 months

Showing 30241–30260 of 47,764 recalls

Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: CarePlus Incubator Ohmeda-Ohio CarePlus Incubator- Incubators provide a...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000/IMMULITE 2000 XPi Systems Prostate-Specific Antigen (PSA)...

The Issue: Siemens Healthcare Diagnostics confirmed that the IMMULITE 2000/ IMMULITE...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Incubator Ohmeda Medical Giraffe Incubator-The Giraffe Incubator is...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE/IMMULITE 1000 Systems Prostate-Specific Antigen (PSA) Assay...

The Issue: Siemens Healthcare Diagnostics has confirmed that the IMMULITE/ IMMULITE...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: FV-RF (Clinix RF Plus) Product Usage: A Stationary X-ray System Recalled by...

The Issue: There's a potential for liquid penetration into the back side of the front...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Incubator The Giraffe Incubator is an infant incubator. Incubators...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Exam Light The Exam Light illuminates body surfaces and Recalled by...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Teleflex Medical

Recalled Item: WECK Visistat 35W Recalled by Teleflex Medical Due to Sterility Deficiency:...

The Issue: Sterility Deficiency: The packages are not sealed properly and thus the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe OmniBed Ohmeda Medical Omnibed- The OmniBed is a combination...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: IWS Infant Warmer System-Infant radiant warmers provide infrared heat...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Bedded Warmer Recalled by Ohmeda Medical Due to Certain power cords...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe OmniBed Ohmeda Medical Giraffe OmniBed- The OmniBed is a Recalled by...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Bedded Warmer Recalled by Ohmeda Medical Due to Certain power cords...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Rocuronium Bromide 50 mg/5 mL Injection Solution Recalled by Cantrell Drug...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Ropivacaine HCl 0.25% in 0.9% Sodium Chloride Recalled by Cantrell Drug...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride (0.2 Recalled by...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Fentanyl Citrate 1 Recalled by Cantrell Drug Company Due to Lack of...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Succinylcholine Chloride 200 mg/10 mL Injection Solution 10 mL (20 mg/mL)...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Heparin Sodium Recalled by Cantrell Drug Company Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Fentanyl Citrate 2 Recalled by Cantrell Drug Company Due to Lack of...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund