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. 2,412 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,412 in last 12 months

Showing 1962119640 of 27,645 recalls

Medical DeviceApril 19, 2016· Elekta, Inc.

Recalled Item: Radionuclide Radiation Therapy System Product The product is a teletherapy...

The Issue: The latches of the frame adapter can be locked even if the locating pins of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2016· Berchtold Corp.

Recalled Item: Surgical Table Cushion (HybriGel Pads) HybrGel Pads are an optional Recalled...

The Issue: The Surgical Table Cushion (HybriGel Pads) could potentially contain staples...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2016· Ortho-Clinical Diagnostics

Recalled Item: The VITROS¿ Chemistry Products Calibrator Kit 31 Recalled by Ortho-Clinical...

The Issue: There is an incorrect value (data/calibration mathematics) on ADDs. This...

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

Class III — Low RiskOngoing
Medical DeviceApril 18, 2016· Synthes (USA) Products LLC

Recalled Item: 3.2 mm Three-fluted drill bit Recalled by Synthes (USA) Products LLC Due to...

The Issue: The sterile packaging may be compromised. A protective cap is to be secured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2016· Synthes (USA) Products LLC

Recalled Item: 3.2 mm three-fluted Radiolucent Drill Bit/Needle Point/145 mm Sterile...

The Issue: The sterile packaging may be compromised. A protective cap is to be secured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Covidien LLC

Recalled Item: Given Imaging Bravo¿ pH capsule delivery device Recalled by Covidien LLC Due...

The Issue: Potential of an allergic reaction in a patient with nickel sensitivity.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Carestream Health Inc

Recalled Item: CARESTREAM Image Suite V3: MINI-PACS/F IMG ST/CLASSIC: REF/Catalog # 1036490...

The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Carestream Health Inc

Recalled Item: CARESTREAM Image Suite V4 Recalled by Carestream Health Inc Due to...

The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Covidien LLC

Recalled Item: Given Imaging Bravo¿¿ pH capsule delivery device Recalled by Covidien LLC...

The Issue: Potential of an allergic reaction in a patient with nickel sensitivity.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...

The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Biomerieux France Chemin De L'Or

Recalled Item: VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated...

The Issue: Due to a packaging error; The kit does not contain the correct number of C1...

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

Class III — Low RiskOngoing
Medical DeviceApril 15, 2016· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...

The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Neff DAgostino Percutaneous Access Set Accessories Recalled by Cook Inc. Due...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Aprima Access Nonvascular Introducer Set Accessories Recalled by Cook Inc....

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Shuttle Select Slip-Cath Catheter Recalled by Cook Inc. Due to Increase in...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Beacon Tip Royal Flush Plus High-Flow Catheter Catheter Recalled by Cook...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: FluoroSet Radiographic Tubal Assessment Set Cannula Recalled by Cook Inc....

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Beacon Tip Torcon NB Advantage Catheter Catheter Recalled by Cook Inc. Due...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Kumpe Access Catheter Cathether Recalled by Cook Inc. Due to Increase in...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Haskal Transjugular Intrahepatic Portal Access Set Introducer Recalled by...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing