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. 2,286 recalls have been distributed to Hawaii in the last 12 months.
Showing 45061–45080 of 47,764 recalls
Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...
The Issue: The test strips in the affected product lots of the OC Light immunological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchron LXi 725 Clinical System Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxC 600i Synchron Access Clinical System Recalled by Beckman Coulter...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...
The Issue: The test strips in the affected product lots of the OC Light immunological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System. Radiation treatment planning. Recalled by Elekta, Inc....
The Issue: The beam is displayed at the "gantry" angle, but the dose is calculated at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANTI-BORRELIA (LYME) MICROPLATE EIA Kit Recalled by Innominata Dba Genbio...
The Issue: Multiple incidents of low-reacting assay plates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pantoprazole Sodium Delayed Release Tablets USP Recalled by Jubilant Cadista...
The Issue: cGMP Deviations: Oral products were not manufactured in accordance with Good...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meprobamate Recalled by Watson Laboratories Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Watson Laboratories Inc. is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meprobamate Recalled by Watson Laboratories Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Watson Laboratories Inc. is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Organic Lemon Grass Tea Bag Cut (TBC) Recalled by Qtrade Teas And Herb Due...
The Issue: QTrade Teas & Herbs is recalling Organic Lemon Grass Tea Bag Cut (TBC)...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zimmer NexPosure Recalled by Zimmer, Inc. Due to Possibility that the inner...
The Issue: Possibility that the inner pouch may be compromised. The product is packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avex CX Suite Recalled by Ultradent Products, Inc. Due to Orthodontic...
The Issue: Orthodontic brackets distributed was incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic DBS Therapy for Dystonia Kit Recalled by Medtronic Neuromodulation...
The Issue: There is a potential for lead damage due to the use of the lead cap provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic DBS Lead Kit for Deep Brain Stimulation Recalled by Medtronic...
The Issue: There is a potential for lead damage due to the use of the lead cap provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Ortho-Clinical...
The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERNAL HEX RECON SCREW Recalled by Smith & Nephew Inc Due to 75 mm screws...
The Issue: 75 mm screws were packaged and labeled using an 80 mm screw outer box and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CR MD1.0 General Set Recalled by AGFA Corp. Due to The cassettes were...
The Issue: The cassettes were shipped with the wrong IP (image plate) size bar code.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Spine Polaris 5.5 Button Lock Screw Inserter. Catalog Number Recalled...
The Issue: Increased risk of failure at the driver tip during screw insertion or removal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.