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. 2,391 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,391 in last 12 months

Showing 2296122980 of 47,764 recalls

Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Hex Driver 1.2 Recalled by TriMed Inc. Due to The epoxy on Apex...

The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Wrist Hook Dorsal Impactor Recalled by TriMed Inc. Due to The WHD/WHV...

The Issue: The WHD/WHV impactors can rust over time due to an improper manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-2000 Analyzer Recalled by Tosoh Bioscience Inc Due to There is a...

The Issue: There is a possibility that the liquid suction pump on some AIA-2000...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Locking Drill Guide Recalled by TriMed Inc. Due to The epoxy on Apex...

The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Siemens Medical Solutions USA, Inc.

Recalled Item: Biograph mCT: a) S(64)-3R Recalled by Siemens Medical Solutions USA, Inc....

The Issue: The terminals on the plug may become loose and overheat.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Peg Guide Extender Recalled by TriMed Inc. Due to The spring on the...

The Issue: The spring on the PEG-Extender can rust due to the type of steel used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-900Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience has...

The Issue: Tosoh Bioscience has become aware of a potential issue with the AIA-900 and...

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

Class II — Potential Health HazardOngoing
DrugSeptember 28, 2018· Tailor Made Compounding

Recalled Item: Tesamorelin Recalled by Tailor Made Compounding Due to Labeling: Incorrect...

The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date; vial indicates a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing