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. 2,322 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,322 in last 12 months

Showing 3996139980 of 47,764 recalls

Medical DeviceJune 3, 2014· DePuy Orthopaedics, Inc.

Recalled Item: RECLAIM Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic...

The Issue: The product can be difficult to remove from the Distal Stem both out of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2014· DePuy Orthopaedics, Inc.

Recalled Item: RECLAIM DISTAL TAPERED Distal Stem Recalled by DePuy Orthopaedics, Inc. Due...

The Issue: The product can be difficult to remove from the Distal Stem both out of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2014· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 500 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential for sample misidentification.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2014· Instrumentation Laboratory Co.

Recalled Item: ACL TOP (Base) Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential for sample misidentification.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2014· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 700 Recalled by Instrumentation Laboratory Co. Due to Potential for...

The Issue: Potential for sample misidentification.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2014· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 700 LAS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential for sample misidentification.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2014· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 700 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential for sample misidentification.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2014· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 300 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential for sample misidentification.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2014· Instrumentation Laboratory Co.

Recalled Item: ACL TOP CTS Recalled by Instrumentation Laboratory Co. Due to Potential for...

The Issue: Potential for sample misidentification.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2014· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System...

The Issue: Covidien is conducting a medical device field correction for specific...

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

Class II — Potential Health HazardOngoing
DrugJune 2, 2014· Alexion Pharmaceuticals, Inc.

Recalled Item: Soliris (eculizumab) Recalled by Alexion Pharmaceuticals, Inc. Due to...

The Issue: Presence of Particulate Matter: Product failed the appearance for the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 2, 2014· Frito-Lay, Inc

Recalled Item: Oven Baked Lay's BBQ flavor crisps in 1 1/8 oz package Recalled by...

The Issue: Printing error by the packaging manufacturer erroneously added a "GF" symbol...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 2, 2014· Maui Soda & Ice Works Ltd/dba Roselani Ice Cream

Recalled Item: Roselani Tropics Kona Mud Mud Pie Ice Cream: 1.75QT Recalled by Maui Soda &...

The Issue: Complaint received of a carton of Roselani Tropics Kona Mud Pie Ice Cream...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra S with 1 #2 Ultrabraid (blue) Product Code: Recalled by...

The Issue: Sterility of device is compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra S with 1 #2 Ultrabraid Suture (blue/white) Product Recalled...

The Issue: Sterility of device is compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra S Double Loaded Suture Product Code: 72203854 Fastener...

The Issue: Sterility of device is compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Blue Product Recalled by...

The Issue: Sterility of device is compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Cobraid Suture Recalled...

The Issue: Sterility of device is compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: MicroScan WalkAway-40 plus Instrument and MicroScan Walkaway-96 plus...

The Issue: Springs contained in the access door hinge assembly on the Walk Away Plus...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare ADVIA Acid/Base Reagent 1 and 2 Kit containing Recalled...

The Issue: Swollen acid bottles due to a trace metal contamination in the Acid Reagent...

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

Class II — Potential Health HazardOngoing