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. 2,512 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,512 in last 12 months

Showing 1232112340 of 47,764 recalls

Medical DeviceMarch 31, 2022· CooperSurgical, Inc.

Recalled Item: Cooper Surgical H/S ELLIPTOSPHERE CATH 5 FR Set-For administering contrast...

The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2022· CooperSurgical, Inc.

Recalled Item: CooperSurgical H/S CATHETER SET FR 5 with Integated Stylet Model: Recalled...

The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2022· Olympus Corporation of the Americas

Recalled Item: Olympus DISPOSABLE GRASPING FORCEPS Recalled by Olympus Corporation of the...

The Issue: Forceps do not comply with Olympus standards for the amount of force...

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

Class II — Potential Health HazardOngoing
DrugMarch 30, 2022· Unilever United States Inc.

Recalled Item: Suave 24-Hour Protection Aerosol Antiperspirant Powder scent Recalled by...

The Issue: Chemical contamination: presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 30, 2022· Unilever United States Inc.

Recalled Item: Suave 24-Hour Protection Aerosol Antiperspirant Fresh scent Recalled by...

The Issue: CGMP Deviation; manufactured at the same facility where other lots were...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 30, 2022· Skippy Foods, LLC.

Recalled Item: SKIPPY Creamy Peanut Butter Blended with Plant Protein NET WT Recalled by...

The Issue: Potential to contain small steel contaminants.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 30, 2022· Skippy Foods, LLC.

Recalled Item: SKIPPY Reduced Fat Chunky Peanut Butter NET WT 16.3 oz Recalled by Skippy...

The Issue: Potential to contain small steel contaminants.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 30, 2022· Skippy Foods, LLC.

Recalled Item: SKIPPY Reduced Fat Creamy Peanut Butter NET WT 40 oz Recalled by Skippy...

The Issue: Potential to contain small steel contaminants.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 30, 2022· Howmedica Osteonics Corp.

Recalled Item: Triathlon Tritanium Tibial Component (Size 6) Recalled by Howmedica...

The Issue: Stryker has discovered a potential product mix where the size of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· Medtronic Neuromodulation

Recalled Item: Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with...

The Issue: The Implantable Neurostimulator Model may be susceptible to not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· Medtronic Neuromodulation

Recalled Item: Percept PC BrainSense Implantable Neurostimulator (INS) Model B35200...

The Issue: The Implantable Neurostimulator (INS) cannot communicate with the clinical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· Invacare Corporation

Recalled Item: Invacare TDX SP2 Recalled by Invacare Corporation Due to The battery wiring...

The Issue: The battery wiring harness on affected wheelchairs may become disconnected...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· Devicor Medical Products Inc

Recalled Item: HydroMARK Breast Biopsy Marker Recalled by Devicor Medical Products Inc Due...

The Issue: Small patient labels do not match the primary device label. The primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· Medtronic Neuromodulation

Recalled Item: Percept BrainSense Implantable Neurostimulator (INS) Recalled by Medtronic...

The Issue: The Implantable Neurostimulator (INS) cannot communicate with the clinical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· Accriva Diagnostics, Inc.

Recalled Item: The VerifyNow P2Y12 Test is designed to measure platelet P2Y12 Recalled by...

The Issue: Two whole blood Platelet Reactivity tests exist that share the same reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· Medtronic Inc

Recalled Item: Instructions for Use Recalled by Medtronic Inc Due to Errors and...

The Issue: Errors and inconsistencies that were identified in the Instruction for Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· Abbott Vascular

Recalled Item: Dragonfly OpStar Imaging Catheter Recalled by Abbott Vascular Due to There...

The Issue: There is a potential that the proximal marker may separate from the imaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 30, 2022· restor3d Inc.

Recalled Item: Evans Wedge Disposable Trials Recalled by restor3d Inc. Due to During...

The Issue: During re-work of disposable instruments to relabel for 4-year shelf-life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· restor3d Inc.

Recalled Item: Non-Sterile Double Ended Trial Kit Recalled by restor3d Inc. Due to Product...

The Issue: Product labeled incorrectly. The lot was labeled with Small footprint when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· restor3d Inc.

Recalled Item: Evans Wedge Disposable Trials Recalled by restor3d Inc. Due to During...

The Issue: During re-work of disposable instruments to relabel for 4-year shelf-life of...

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

Class II — Potential Health HazardOngoing