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. 1,682 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
1,682 in last 12 months

Showing 4036140380 of 47,764 recalls

FoodMay 16, 2014· Kraft Foods Group

Recalled Item: Low fat cottage cheese Recalled by Kraft Foods Group Due to Kraft Foods is...

The Issue: Kraft Foods is voluntarily recalling 18 SKUs of Knudsen Cottage Cheese, nine...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2014· Kraft Foods Group

Recalled Item: Cottage cheese Recalled by Kraft Foods Group Due to Kraft Foods is...

The Issue: Kraft Foods is voluntarily recalling 18 SKUs of Knudsen Cottage Cheese, nine...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2014· Kraft Foods Group

Recalled Item: Fat free cottage cheese sold under the Knudsen or Kraft Recalled by Kraft...

The Issue: Kraft Foods is voluntarily recalling 18 SKUs of Knudsen Cottage Cheese, nine...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2014· Kraft Foods Group

Recalled Item: Cottage Doubles - cottage cheese Recalled by Kraft Foods Group Due to Kraft...

The Issue: Kraft Foods is voluntarily recalling 18 SKUs of Knudsen Cottage Cheese, nine...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2014· Kraft Foods Group

Recalled Item: Cottage Doubles - cottage cheese Recalled by Kraft Foods Group Due to Kraft...

The Issue: Kraft Foods is voluntarily recalling 18 SKUs of Knudsen Cottage Cheese, nine...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2014· Kraft Foods Group

Recalled Item: Low fat cottage cheese Recalled by Kraft Foods Group Due to Kraft Foods is...

The Issue: Kraft Foods is voluntarily recalling 18 SKUs of Knudsen Cottage Cheese, nine...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2014· Kraft Foods Group

Recalled Item: Cottage Doubles - cottage cheese Recalled by Kraft Foods Group Due to Kraft...

The Issue: Kraft Foods is voluntarily recalling 18 SKUs of Knudsen Cottage Cheese, nine...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2014· Kraft Foods Group

Recalled Item: Cottage cheese Recalled by Kraft Foods Group Due to Kraft Foods is...

The Issue: Kraft Foods is voluntarily recalling 18 SKUs of Knudsen Cottage Cheese, nine...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2014· Hospira Inc.

Recalled Item: Labetalol Hydrochloride Injection Recalled by Hospira Inc. Due to Presence...

The Issue: Presence of Particulate Matter; metal embedded in the glass vial and visible...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2014· US Compounding Inc

Recalled Item: ePHEDrine Sulfate Injection Recalled by US Compounding Inc Due to Mislabeling

The Issue: Labeling: Label Error on Declared Strength; The outer light protective bags,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2014· Actavis Inc

Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug.

The Issue: Subpotent Drug.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 16, 2014· Ventlab LLC

Recalled Item: Manual Resuscitator Bag Series: AF1000 Recalled by Ventlab LLC Due to The...

The Issue: The pop-off valve in the defective devices remain open and a squeeze of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 16, 2014· Alcon Research, Ltd.

Recalled Item: Alcon CUSTOM-PAK containing Anterior Chamber Cannula 27G Component Part...

The Issue: Alcon CUSTOM-PAK which is supposed to contain a 27G Anterior Chamber Cannula...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2014· Nidek Inc

Recalled Item: GYC-1000 Green Laser Photocoagulator system The Nidek Green Laser...

The Issue: Laser Aperture label was not applied to certain GYC-1000 Green Laser...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Biomet, Inc.

Recalled Item: DISCOVERY ELBOW prosthesis Recalled by Biomet, Inc. Due to Surface finish is...

The Issue: Surface finish is different than specified. The implant has 30 grit blast on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips MR systems: Trolley Variable Height IRF (for Ingenia 1.5T Recalled...

The Issue: Ingenia customers have experienced clamping of the foot under the central...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Ebi, Llc

Recalled Item: Biomet Spine Recalled by Ebi, Llc Due to The Cypher MIS Screw Inserter may...

The Issue: The Cypher MIS Screw Inserter may exhibit an increased rate of instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips MR systems: Ingenia HA FLEX TRAK Trolley (for Ingenia Recalled by...

The Issue: Ingenia customers have experienced clamping of the foot under the central...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing