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. 2,293 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,293 in last 12 months

Showing 4230142320 of 47,764 recalls

DrugOctober 9, 2013· Sandoz, Inc

Recalled Item: Ropinirole Recalled by Sandoz, Inc Due to Cross contamination with other...

The Issue: Cross contamination with other products: Sandoz is recalling certain lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2013· Actavis Elizabeth LLC

Recalled Item: Alprazolam Orally Disintegrating Tablets Recalled by Actavis Elizabeth LLC...

The Issue: Failed Tablet/Capsule Specifications; partial tablet erosion resulting in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 8, 2013· Ortho-Clinical Diagnostics

Recalled Item: enGen Track System with enGen Select v5.0 with autoverification enabled...

The Issue: Ortho Clinical Diagnostics issued an Urgent Product Correction Notification...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Implant Holder for Synfix (TM)-LR the Synthes Implant Holder...

The Issue: Complaints were received which described the SynFix LR implant holder...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2013· Ortho-Clinical Diagnostics

Recalled Item: enGen Track System with enGen Custom v3.2.2 (& below) Product The VITROS 5...

The Issue: Ortho Clinical Diagnostics issued an Urgent Product Correction Notification...

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

Class II — Potential Health HazardOngoing
FoodOctober 8, 2013· Quaker Foods and Snacks North America

Recalled Item: White grits packaged in a paper bag labeled in part: Smooth & Creamy...

The Issue: Some Aunt Jemima brand Buttermilk Self-Rising Corn Meal Mix, Quick Grits...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 8, 2013· Quaker Foods and Snacks North America

Recalled Item: White grits packaged in a paper bag labeled in part: Smooth & Creamy...

The Issue: Aflatoxins. Some Aunt Jemima brand Buttermilk Self-Rising Corn Meal Mix,...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 7, 2013· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Multi Parameter Patient Monitor (with Arrhythmia Detection and Alarms)...

The Issue: Mindray has identified an issue with V Series Monitor where the V Dock power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2013· Smith & Nephew Inc

Recalled Item: GENESIS(R) II Recalled by Smith & Nephew Inc Due to Swapped product....

The Issue: Swapped product. Non-porous tibial base size 5 L was mis-packaged as size 6...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: User Defined Method Flex Assignment/Siemens Dimension Vista 500 or Dimension...

The Issue: When utilizing the Routine Inventory screen to enter a User Defined Method...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2013· RTI Surgical, Inc.

Recalled Item: C-Plus" 10mm x 12mm Webless implants Pioneer Surgical's C-Plus " Recalled by...

The Issue: As the result of a recent internal review of regulatory documents, we have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2013· Medtronic Vascular, Inc.

Recalled Item: Resolute Integrity Zotarolimus-eluting Coronary Stent: Stent ID 3.0 mm...

The Issue: A small number of units in lot number 0006573585 of the Resolute Integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2013· Smith & Nephew Inc

Recalled Item: GENESIS(R) II Recalled by Smith & Nephew Inc Due to Swapped product....

The Issue: Swapped product. Non-porous tibial base size 5 L was mis-packaged as size 6...

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

Class II — Potential Health HazardOngoing
DrugOctober 7, 2013· B @ B Trade Inc.

Recalled Item: Lidiy capsules Dietary Supplement. Each bottle contains 30 capsules....

The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 7, 2013· B @ B Trade Inc.

Recalled Item: Slim Fortune capsules Dietary Supplement. Each bottle contains 30 capsules....

The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 7, 2013· Amedra Pharmaceuticals LLC

Recalled Item: Dexedrine¿ (Dextroamphetamine Sulfate) Spansules¿ Sustained Release Capsules...

The Issue: Failed Dissolution Specifications: Out of Specification (OOS) test results...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2013· B @ B Trade Inc.

Recalled Item: Slim Expert softgel capsules Dietary Supplement. One month supply/ 30...

The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 7, 2013· Baxter Healthcare Corp.

Recalled Item: 1) The HomeChoice automated peritoneal dialysis system. Dataplate located on...

The Issue: In systems with version 10.4 software Initial Drain logic, the device will...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products COCM Reagent Recalled by Ortho-Clinical...

The Issue: Inaccurate quality control results.

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

Class II — Potential Health HazardOngoing
FoodOctober 4, 2013· Ultra Laboratories

Recalled Item: Digestive Health Recalled by Ultra Laboratories Due to Ultra Laboratories is...

The Issue: Ultra Laboratories is recalling Digestive Health because a raw material used...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund