Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,506 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,506 in last 12 months

Showing 1086110880 of 46,762 recalls

Medical DeviceAugust 3, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE CLEARPRO TRACH DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by...

The Issue: Potential for the suction catheter to come apart from the green connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by MEDLINE...

The Issue: Potential for the suction catheter to come apart from the green connector...

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

Class II — Potential Health HazardOngoing
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 2, 2022· CIPLA

Recalled Item: Difluprednate Ophthalmic Emulsion 0.05% Recalled by CIPLA Due to Lack of...

The Issue: Lack of Assurance of Sterility: Complaints received of defective container...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 2, 2022· Carwild Corporation

Recalled Item: FABCO ORS DENTAL ROLLS Recalled by Carwild Corporation Due to Sterility with...

The Issue: Sterility with new cotton source not validated

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

Class II — Potential Health HazardOngoing
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· 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: 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: 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· 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 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" (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· 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
DrugJuly 29, 2022· Edgewell Personal Care Brands, LLC

Recalled Item: Banana Boat hair & scalp defense Recalled by Edgewell Personal Care Brands,...

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
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6028...

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 Catalog Number: 6501...

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: 4575-OLY 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: Freeman Pancreatic Flexi-Stent Kit (containing 6533) Catalog Number: 6507...

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 Transbronchial Aspiration Needle Catalog Number: 4621 Recalled 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