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. 2,538 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,538 in last 12 months

Showing 1058110600 of 47,764 recalls

Medical DeviceOctober 21, 2022· Howmedica Osteonics Corp.

Recalled Item: Simplex HV With Gentamicin CE Recalled by Howmedica Osteonics Corp. Due to...

The Issue: Simplex HV With Gentamicin CE, 10 PACKS (P/N 6193-1-010) were distributed to...

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

Class II — Potential Health HazardOngoing
FoodOctober 20, 2022· Seed Ranch Flavor Co

Recalled Item: Umami Everyday Savory Spice Recalled by Seed Ranch Flavor Co Due to...

The Issue: Three sauces contain undeclared soy.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 20, 2022· Seed Ranch Flavor Co

Recalled Item: Everything But The Sushi & Dumplings Recalled by Seed Ranch Flavor Co Due to...

The Issue: Three sauces contain undeclared soy.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 20, 2022· Seed Ranch Flavor Co

Recalled Item: Umami Everyday Sauce Recalled by Seed Ranch Flavor Co Due to Undeclared Soy

The Issue: Three sauces contain undeclared soy.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 20, 2022· CoreLink LLC

Recalled Item: CoreLink LLC Recalled by CoreLink LLC Due to Specific lots of FLXfit...

The Issue: Specific lots of FLXfit implants have internal components that may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Sensititre Plate Recalled by Remel Inc Due to An internal...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· CooperSurgical, Inc.

Recalled Item: NEO-fit Neonatal Endotracheal Tube Grip Recalled by CooperSurgical, Inc. Due...

The Issue: Firm has received 11 complaints involving a loose or detached metal clips,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2022· Bio-Rad Laboratories, Inc.

Recalled Item: CMV IgM EIA Recalled by Bio-Rad Laboratories, Inc. Due to Due to an unusual...

The Issue: Due to an unusual increase in the positivity rate with human IgM antibodies...

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

Class II — Potential Health HazardOngoing
DrugOctober 18, 2022· Genentech Inc

Recalled Item: Susvimo (ranibizumab injection) Recalled by Genentech Inc Due to Defective...

The Issue: Defective Delivery System: Commercial implants do not meet the filed...

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

Class III — Low RiskOngoing
Refund
DrugOctober 18, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg Recalled by SUN...

The Issue: Presence of Foreign Substance

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 18, 2022· G FUEL LLC

Recalled Item: GFUEL brand Watermelon Limeade Energy Drink Recalled by G FUEL LLC Due to...

The Issue: Product label does not declare the correct amount of caffeine.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 18, 2022· Atrium Medical Corporation

Recalled Item: Atrium Ocean Wet Suction Water Seal Chest Drain- Product Code: 2002-000...

The Issue: Warehouse experienced temperature excursions in July and August 2021. It was...

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

Class II — Potential Health HazardOngoing