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. 2,470 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,470 in last 12 months

Showing 1712117140 of 27,645 recalls

Medical DeviceJune 22, 2017· Medtronic Perfusion Systems

Recalled Item: DLP Pressure Disposable Pressure Display Sets Extends the pressure line...

The Issue: Identification of small pinholes in a single packaging configuration of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· NeuroLogica Corporation

Recalled Item: The GC80 Digital X-ray Imaging System Recalled by NeuroLogica Corporation...

The Issue: An image was obtained with over exposure during a Thorax examination using...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Driver Shaft (5Hex Recalled by Valorem Surgical LLC Due to...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Spinal & Epidural Anesthesia Tray. Product Catalog Number: 555172. Local...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Perifix Continuous Epidural Anesthesia Tray. Product Catalog Numbers: 332075...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Perifix Epidural AnesthesiaTray. Product Catalog Numbers: 551879 Recalled by...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: PENCAN Spinal Anesthesia Tray. Product Catalog Number: 560590. Local...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Perifix Single Dose Epidural Anesthesia Tray. Product Catalog Number:...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Perifix FX Epidural Anesthesia Tray. Product Catalog Numbers: 551993...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Customer Epidural Anesthesia Tray. Product Catalog Number: 555234. Local...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Pencan Spinal Needle Tray. Product Catalog Number: 333865. Local anesthesia...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Pain Management Tray. Product Catalog Number: 560602. Local anesthesia of...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Contiplex Nerve Block Tray. Product Catalog Number: 570205. Local anesthesia...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 350 Straight Rod. Part of MAXIMIS Pedicle Screw Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS MIS Screw5.5 x 55mm. Part of MAXIMIS Pedicle Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Body Alignment Driver. Part of MAXIMIS Pedicle Screw...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 40mm Rod. Part of MAXIMIS Pedicle Screw Spinal Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 60mm MIS Rod. Part of MAXIMIS Pedicle Screw Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS MIS Screw 6.5 x 40mm and 6.5 x Recalled by Valorem Surgical...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 5.5 x 35mm Curved Rod. Part of MAXIMIS Recalled by Valorem...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing