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. 1,077 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
1,077 in last 12 months

Showing 10921–10940 of 47,764 recalls

DrugAugust 2, 2022· HERON THERAPEUTICS, INC.

Recalled Item: Zynrelef (bupivacaine and meloxicam) Recalled by HERON THERAPEUTICS, INC....

The Issue: Defective Delivery System: An incorrect 10 mL (12 mL) Luer (slip) syringe...

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

Class III — Low RiskOngoing
Refund
DrugAugust 1, 2022· Akorn, Inc

Recalled Item: PrednisoLONE Oral Solution USP Recalled by Akorn, Inc Due to Defective...

The Issue: Defective Container: Product has incomplete induction seals.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: MicroClave Clear Neutral Connector Recalled by ICU Medical, Inc. Due to Due...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· MERCHSOURCE LLC

Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...

The Issue: Excessive ultraviolet-C radiation

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: 6.5" (17 cm) Appx 0.84 ml Recalled by ICU Medical, Inc. Due to Due to a...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· Randox Laboratories Ltd.

Recalled Item: The Randox Serology I Positive Control contains the following analytes...

The Issue: ***Update** :HBsAg analyte is also Non-Reactive on the Ortho Vitros analyser...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: MicroClave Clear Neutral Connector. A bidirectional connector used as an...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: 8.5" (22 cm) Appx 0.85 ml Recalled by ICU Medical, Inc. Due to Due to a...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: 6.5 IN (17 cm) APPX 0.78 ml Recalled by ICU Medical, Inc. Due to Due to a...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: 6" (15 cm) Appx 0.85 ml Recalled by ICU Medical, Inc. Due to Due to a...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Medical Cytology Brush Catalog Number: 4204 Recalled by Hobbs Medical,...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Freeman Pancreatic Flexi-Stent Catalog Number: 6566 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Posi-Stop Injection Needle Catalog Number: 4712 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 4563 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Medical Flex-Ez Guide Wire Disposable For endoscopy procedures by...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Biliary Pigtail Stent Kits (containing 6105) Catalog Number: 6023...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Freeman Pancreatic Flexi-Stent Kits: Single Pigtail (containing 6544)...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Posi-Stop Injection Needle Catalog Number: 4720 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Biliary Pigtail Stent Kits Catalog Number: 6105 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Helical Retrieval Basket Catalog Number: 4814 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing