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 1664116660 of 27,645 recalls

Medical DeviceOctober 11, 2017· Zimmer Dental Inc

Recalled Item: Zimmer Dental Tapered SwissPlus & SwissPlus Implant Systems surgical kit...

The Issue: The device may contain a manufacturing condition affecting the geometry of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Spacelabs Healthcare, Ltd.

Recalled Item: Arkon Anesthesia Delivery System Recalled by Spacelabs Healthcare, Ltd. Due...

The Issue: Arkon Anesthesia Workstation, with software version 2.61, experienced...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Dental Inc

Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...

The Issue: The device may contain a manufacturing condition affecting the geometry of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Dental Inc

Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...

The Issue: The device may contain a manufacturing condition affecting the geometry of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Biomet, Inc.

Recalled Item: TunneLoc Tibial Fixation Device Product Usage: To provide fixation of...

The Issue: Gamma sterilization validation testing indicates the sterilization dose for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2017· Karl Storz Endoscopy

Recalled Item: STORZ High Flow Insufflation Tubing (with filter) Recalled by Karl Storz...

The Issue: The label outside the cardboard box is labeled correctly but the pouches...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: ImplantDirect Legacy(TM) 3 Implant Recalled by Implant Direct Sybron...

The Issue: One reported complaint and discovered that the outer vial was out of round...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2017· Crimson Trace Corporation

Recalled Item: Crimson Trace Corporation laser sights. The Finished Products are laser...

The Issue: A previously "in specification" Finished Product with a Model 25-0657 diode...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· CooperSurgical, Inc.

Recalled Item: Cooper Surgical 2 MHZ Waterproof OB Probe Product The CooperSurgical...

The Issue: The 2MHZ prove was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Allen Medical Systems

Recalled Item: Radiolucent Surgery Spine Frame (F70801). Surgical platform used to position...

The Issue: The base of the frame has the potential to crack when the patient is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Allen Medical Systems

Recalled Item: Allen Medical Bow Frame Model A-70800. Surgical platform used to Recalled by...

The Issue: The base of the frame has the potential to crack when the patient is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults with BALLARD Technology WET...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: NOVAPLUS* Endotracheal WET PAK* Closed Suction System for Adults with...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing