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. 2,550 recalls have been distributed to Alaska in the last 12 months.
Showing 2861–2880 of 46,762 recalls
Recalled Item: PHENYLephrine added to 0.9% sodium chloride Recalled by Central Admixture...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Connecta BD Luer-Lok 360 Recalled by BD SWITZERLAND SARL Due to Due to...
The Issue: Due to specific lots of luer-lok devices were shipped to the U.S. market...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device...
The Issue: The product is mislabeled with the incorrect anterior height of 10mm, but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite Inactivated Standard: Inactivated Influenza A/B and Respiratory...
The Issue: The RSV target may give a late Ct value and could potentially not pass QC.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus...
The Issue: The A549 human cell target (human cells for sample adequacy control) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT...
The Issue: There is a potential for the sterility of the device to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wayson Hydrocolloid Models: 1) Model Number: CUR5103 Recalled by MEDLINE...
The Issue: There is a potential for the sterility of the device to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVAC Aspiration System Recalled by Calyxo, Inc. Due to Aspiration system,...
The Issue: Aspiration system, for endoscopic examination/treatment of urinary tract and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIM software Recalled by MIM Software Inc Due to In situations where two...
The Issue: In situations where two images with differing Fields of View (FOV) complete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe Recalled by Turbare Manufacturing...
The Issue: Lack of Assurance of Sterility: due to a quality control process deviation....
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CURAD Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ergocalciferol - Vitamin D Supplement - 10 mcg (400 Units) Recalled by...
The Issue: Defective Delivery System: Leakage observed after oral solution was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam 0.5 mg per 0.25 mL Oral Syringe Recalled by Safecor Health, LLC...
The Issue: Defective Delivery System: Leakage observed after oral solution was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ferrous Sulfate 7.5 mg Iron/0.5 mL Oral Syringe Recalled by Safecor Health,...
The Issue: Defective Delivery System: Leakage observed after oral solution was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate 5 mg per 0.25 mL Oral Syringe Recalled by Safecor Health,...
The Issue: Defective Delivery System: Leakage observed after oral solution was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simethicone 20 mg per 0.3 mL Oral Syringe Recalled by Safecor Health, LLC...
The Issue: Defective Delivery System: Leakage observed after oral solution was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Initiation 18 Coated Regular and 18 Coated Super Tampons Recalled by DAYE...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 18 Coated Regular and 18 Nude Regular Tampons Recalled by DAYE...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18 Coated Regular and 18 Nude Regular Tampons Recalled by DAYE (ANNE'S DAY...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.