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. 1,077 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
1,077 in last 12 months

Showing 8601–8620 of 47,764 recalls

Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE NON-STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Affected product lots were mislabeled as "STERILE PVP SLN" when they should...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE NON-STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Affected product lots were mislabeled as "STERILE PVP SLN" when they should...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE NON-STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Affected product lots were mislabeled as "STERILE PVP SLN" when they should...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Baxter Healthcare Corporation

Recalled Item: Allen Advance Chest Support with Pad Recalled by Baxter Healthcare...

The Issue: Potential for the device to crack where the Chest Base Prone support...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE NON-STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Affected product lots were mislabeled as "STERILE PVP SLN" when they should...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE NON-STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Affected product lots were mislabeled as "STERILE PVP SLN" when they should...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE NON-STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Affected product lots were mislabeled as "STERILE PVP SLN" when they should...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE NON-STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Affected product lots were mislabeled as "STERILE PVP SLN" when they should...

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

Class II — Potential Health HazardOngoing
DrugMay 18, 2023· Aurolife Pharma, LLC

Recalled Item: Glycopyrrolate Tablets Recalled by Aurolife Pharma, LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
FoodMay 17, 2023· HU PRODUCTS

Recalled Item: Hu Vanilla Crunch Dark Chocolate bar Recalled by HU PRODUCTS Due to...

The Issue: may contain undeclared tree-nuts

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 16, 2023· Heartware, Inc.

Recalled Item: HeartWare Ventricular Assist Device System. a) Monitor 1521US Explore Tech...

The Issue: Medtronic has identified that the logfiles downloaded from the recently...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2023· Draeger Medical Systems, Inc.

Recalled Item: Draeger Softbed Resuscitaire and/or Birthing Room Warmer with Scale...

The Issue: The Resuscitaire Infant Radiant Warmer with the optional scale could display...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Aptio Automation Storage and Retrieval Module (SRM) Recalled by Siemens...

The Issue: A firmware error may lead to an incorrect association of test result(s) to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2023· Bryan Medical Inc

Recalled Item: Aeris Balloon Dilation Catheter Recalled by Bryan Medical Inc Due to Mislabeling

The Issue: Devices were mislabeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· Olympus Corporation of the Americas

Recalled Item: Always-On Tip Tracked Instruments (SPiN Drive instruments) 21ga ANSO...

The Issue: Electromagnetic (EM) sensor tracking malfunction impacts the use of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· GE OEC Medical Systems, Inc

Recalled Item: Field Upgrade Kits: P/N 5451208 RIU Recalled by GE OEC Medical Systems, Inc...

The Issue: Image intensifiers on systems, used to provide fluoroscopic/digital spot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing Turkuaz Ultrasound Gel Recalled by...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing