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. 2,549 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,549 in last 12 months

Showing 65816600 of 47,764 recalls

Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Brasseler USA I Lp

Recalled Item: Brasseler 8S RA SHP RD (Super-Sharp Round) H1S.21.023 Recalled by Brasseler...

The Issue: The device has a grip detail (right angle latch) out of specification...

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

Class II — Potential Health HazardOngoing
FoodJanuary 10, 2024· Big Island Candies, Inc.

Recalled Item: Makana Brownie Assortment Box Golden Macadamia Nut Brownie Milk Chocolate...

The Issue: Wrong product in package; undeclared allergen (peanuts)

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 10, 2024· Now Foods

Recalled Item: Protocol for Life Balance Recalled by Now Foods Due to Amount of...

The Issue: Amount of Phosphatidyl Serine in product is less than stated on the label

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

Class III — Low RiskOngoing
Refund
DrugJanuary 10, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Remedy Clinical TREAT Antifungal Cream Recalled by MEDLINE...

The Issue: Labeling: Not Elsewhere Classified; Product labeling contains the claim of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2024· BE PHARMACEUTICALS AG

Recalled Item: Fosaprepitant for Injection 150 mg per vial Recalled by BE PHARMACEUTICALS...

The Issue: Lack of Sterility Assurance: Aseptic process simulation failure.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 10, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse PACS - Version 7.2.100 Recalled by FUJIFILM Healthcare Americas...

The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse PACS - Version 7.1.000 Recalled by FUJIFILM Healthcare Americas...

The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse PACS - Version 7.2.000 Recalled by FUJIFILM Healthcare Americas...

The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse PACS - Version 7.1.000US Recalled by FUJIFILM Healthcare Americas...

The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse PACS - Version 7.3.000 Recalled by FUJIFILM Healthcare Americas...

The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse PACS - Version 7.2.200 Recalled by FUJIFILM Healthcare Americas...

The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...

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

Class II — Potential Health HazardOngoing