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. 2,333 recalls have been distributed to Alaska in the last 12 months.
Showing 32481–32500 of 46,762 recalls
Recalled Item: Xcela Hybrid PICC with PASV Valve Technology Recalled by Navilyst Medical,...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaxcel PICC with PASV Introducer Kit under the following labels: 1) 4F...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFlo Hybrid PICC with ENDEXO and PASV Valve Technology Recalled by...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xcela Hybrid PICC with PASV Valve Technology Recalled by Navilyst Medical,...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaxcel PICC with PASV IR-145 Kit under the following labels: 1) 4F Recalled...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xcela Hybrid PICC with PASV Valve Technology Recalled by Navilyst Medical,...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 Cardiopulmonary bypass on-line...
The Issue: Specific CDI¿ Blood Parameter Monitoring System 500 devices are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaxcel PICC with PASV Introducer Kit under the following labels: 1) 4F...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Formula 2 (Papaverine 9 mg Recalled by Meditech Laboratories, Inc Due to...
The Issue: Superpotent Drug: one ingredient was found to be above assay specification.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Sulfate Tablets USP Recalled by Impax Laboratories, Inc....
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Sulfate Tablets USP Recalled by Impax Laboratories, Inc....
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formula 4 (Papaverine 18 mg Recalled by Meditech Laboratories, Inc Due to...
The Issue: Lack of Assurance of Sterility: incomplete or missing data regarding production.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formula 0 (PGE 20 mcg/mL) Injection Recalled by Meditech Laboratories, Inc...
The Issue: Lack of Assurance of Sterility: incomplete or missing data regarding production.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formula 9 (Papaverine 0.9 mg Recalled by Meditech Laboratories, Inc Due to...
The Issue: Lack of Assurance of Sterility: incomplete or missing data regarding production.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formula 3 (Papaverine 20 mg Recalled by Meditech Laboratories, Inc Due to...
The Issue: Stability Does Not Support Expiry: manufactured with an active ingredient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formula 1 (Papaverine 1.8 mg Recalled by Meditech Laboratories, Inc Due to...
The Issue: Stability Does Not Support Expiry: manufactured with an active ingredient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formula 2 (Papaverine 9 mg Recalled by Meditech Laboratories, Inc Due to...
The Issue: Stability Does Not Support Expiry: manufactured with an active ingredient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SODIUM IODIDE I 131 CAPSULE Recalled by Jubilant Draximage Inc Due to...
The Issue: Labeling: Label Error on Declared Strength
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.