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 1010110120 of 47,764 recalls

Medical DeviceDecember 12, 2022· Medtronic Perfusion Systems

Recalled Item: Custom Pack Perfusion Tubing Packs containing Affinity Fusion Oxygenator...

The Issue: An upward trend of complaints in which the Temperature Monitoring Adapter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Medtronic Perfusion Systems

Recalled Item: Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance...

The Issue: An upward trend of complaints in which the Temperature Monitoring Adapter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Roche Diagnostics Operations, Inc.

Recalled Item: cobas infinity central lab Recalled by Roche Diagnostics Operations, Inc....

The Issue: A complaint investigation revealed that an incorrect behavior relating to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· DeRoyal Industries Inc

Recalled Item: DeRoyal ORGAN RECOVERY PACK PGYBK Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedBank System - Product Label/labeling pending Recalled by...

The Issue: Due to customer complaints related to the MedBank software which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Steris Corporation

Recalled Item: VERIFY Steam Test Pack (20 Tests and 20 controls) Item Recalled by Steris...

The Issue: Biological indicator (BI) used to promote growth of the G....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Steris Corporation

Recalled Item: VERIFY Dual Species Self-Contained Biological Indicators Recalled by Steris...

The Issue: Biological indicator (BI) used to promote growth of the G....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Steris Corporation

Recalled Item: VERIFY Steam Test Pack (20 Tests and 5 controls) Item Recalled by Steris...

The Issue: Biological indicator (BI) used to promote growth of the G....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Steris Corporation

Recalled Item: VERIFY Dual Species Self-Contained Biological Indicators Recalled by Steris...

The Issue: Biological indicator (BI) used to promote growth of the G....

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

Class II — Potential Health HazardOngoing
FoodDecember 11, 2022· ByHeart, INC.

Recalled Item: By Heart Whole Nutrition Infant Formula Recalled by ByHeart, INC. Due to...

The Issue: Infant formula potentially contaminated with Cronobacter sakazakii

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 9, 2022· NCH Life Sciences LLC

Recalled Item: Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Recalled by NCH Life...

The Issue: CGMP Deviations: Impurities of acetal and acetaldehyde were discovered in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 9, 2022· Smiths Medical ASD Inc.

Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...

The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 9, 2022· Smiths Medical ASD Inc.

Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...

The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 9, 2022· Smiths Medical ASD Inc.

Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...

The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 9, 2022· Smiths Medical ASD Inc.

Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...

The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 9, 2022· Smiths Medical ASD Inc.

Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...

The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...

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

Class I — Serious Health HazardOngoing
DrugDecember 8, 2022· McGuff Compounding Pharmacy Services, Inc.

Recalled Item: Thiamine Hydrochloride 200 mg/2mL (100mg/mL) Recalled by McGuff Compounding...

The Issue: Presence of Particulate Matter: Presence of foreign substances were reported...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2022· McGuff Compounding Pharmacy Services, Inc.

Recalled Item: Thiamine Hydrochloride 3000 mg/30 mL (100mg/mL) Recalled by McGuff...

The Issue: Presence of Particulate Matter: Presence of foreign substances were reported...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 8, 2022· TELEFLEX LLC

Recalled Item: Endotracheal Tube labeled as the following: a. Flexi-Set Cuffed Endotracheal...

The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2022· TELEFLEX LLC

Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.

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

Class II — Potential Health HazardOngoing