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. 1,057 recalls have been distributed to Alaska in the last 12 months.
Showing 10861–10880 of 46,762 recalls
Recalled Item: stryker EVOLVE Recalled by Wright Medical Technology, Inc. Due to The outer...
The Issue: The outer label does not match the device inside the package. The affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker EVOLVE Recalled by Wright Medical Technology, Inc. Due to The outer...
The Issue: The outer label does not match the device inside the package. The affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe...
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.
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.
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.
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.
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.
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.