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. 2,372 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,372 in last 12 months

Showing 3150131520 of 47,764 recalls

FoodJuly 19, 2016· Gourmet Foods, Inc.

Recalled Item: Artichoke Heart Breaded with Goat and Cheddar Cheese : Pack Recalled by...

The Issue: Food products were manufactured using flour that has been recalled by...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 19, 2016· Gourmet Foods, Inc.

Recalled Item: Artichoke Heart with Boursin Mousse Breaded Pack Size: 200 ea. Recalled by...

The Issue: Food products were manufactured using flour that has been recalled by...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 19, 2016· Gourmet Foods, Inc.

Recalled Item: Shrimp Coconut Brochette Pack Size: 156 ea. per case Recalled by Gourmet...

The Issue: Food products were manufactured using flour that has been recalled by...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 19, 2016· Gourmet Foods, Inc.

Recalled Item: Shrimp 21/25 Coconut Butterfly Pack Size: 200 ea. per case Recalled by...

The Issue: Food products were manufactured using flour that has been recalled by...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 19, 2016· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Whipknot Soft Tissue Cinch (USP#5) suture. PN: Recalled by...

The Issue: Sterility compromised due to breach in sterile packaging

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2016· Philips Electronics North America Corporation

Recalled Item: MultiDiagnost Eleva Recalled by Philips Electronics North America...

The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2016· Philips Electronics North America Corporation

Recalled Item: UroDiagnost Recalled by Philips Electronics North America Corporation Due to...

The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2016· Philips Electronics North America Corporation

Recalled Item: MultiDiagnost Eleva with Flat Detector Recalled by Philips Electronics North...

The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...

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

Class II — Potential Health HazardOngoing
DrugJuly 18, 2016· GlaxoSmithKline, LLC

Recalled Item: Bactroban Cream Recalled by GlaxoSmithKline, LLC Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2016· GlaxoSmithKline, LLC

Recalled Item: Bactroban Ointment Recalled by GlaxoSmithKline, LLC Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2016· GlaxoSmithKline, LLC

Recalled Item: Bactroban Nasal Recalled by GlaxoSmithKline, LLC Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2016· GlaxoSmithKline, LLC

Recalled Item: Bactroban Cream Recalled by GlaxoSmithKline, LLC Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 18, 2016· J&D's Down Home Enterprises, Inc.

Recalled Item: Original Bacon Flavored Seasoning Salt Recalled by J&D's Down Home...

The Issue: Original Bacon Flavored Seasoning Salt, Big Pig brand, is recalled due to a...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 18, 2016· Aribex Inc

Recalled Item: NOMAD Pro Packaged X-Ray System Recalled by Aribex Inc Due to Firm received...

The Issue: Firm received customer complaints where end users reported that Nomad Pro...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Aribex Inc

Recalled Item: NOMAD Pro2 Packaged X-Ray System Recalled by Aribex Inc Due to Firm received...

The Issue: Firm received customer complaints where end users reported that Nomad Pro...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-450NR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-330BR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-450BR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-330NR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD) Recalled by Becton, Dickinson...

The Issue: Internal review found that some vials of CD3/CD4/CD45 state that the product...

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

Class III — Low RiskOngoing