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 2298123000 of 47,764 recalls

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· GE Healthcare, LLC

Recalled Item: Touchscreen display kit. Sold under the following product names: TOUCHSCREEN...

The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...

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· GE Healthcare, LLC

Recalled Item: Aisys Anesthesia System. Sold under the following product names: AISYS...

The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· GE Healthcare, LLC

Recalled Item: Aisys CS2 Anesthesia System. Sold under the following product names: AISYS...

The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...

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