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. 2,353 recalls have been distributed to Alaska in the last 12 months.
Showing 22741–22760 of 27,254 recalls
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano TrakBack II Disposable Pullback Device Recalled by Volcano...
The Issue: Internal testing had identified a potential breach to the sterile barrier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EZ Negative Pressure Wound Therapy (NPWT) System (RENASYS EZ)...
The Issue: Modification were made to the RENASYS EZ NPWT Systems without a 510(k) or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Water may leak...
The Issue: Water may leak into the center gas lumen of the Patient Circuit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V5Ms Transesophageal transducers Recalled by Siemens Medical Solutions USA,...
The Issue: Reports of deterioration of material covering the articulating section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Immunoassay System Recalled by Siemens Healthcare Diagnostics...
The Issue: The firm is conducting a field correction for the ADVIA Centaur and ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eXpertDC intraoral x-ray Recalled by Gendex Corp Due to Two (2) failures of...
The Issue: Two (2) failures of the spring link components within the articulated arm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Luminos dRF system with SW VD10 or on Luminos Recalled by Siemens...
The Issue: It was determined that a potential malfunction may occur on the Luminos dRF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model...
The Issue: The device may have a non-conforming component that may cause the device to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA Magnesium RTU Reagent Recalled by Horiba Instruments, Inc dba...
The Issue: Horiba Medical is recalling the ABX PENTRA Magnesium RTU Reagent because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENVOY 500 AST Reagent Kit Recalled by ELITech Clinical Systems SAS Due to...
The Issue: Some users of ENVOY 500 AST Reagent Kit, 55255, for Envoy 500 systems are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent Titamax WS Cortical Implant ¿4.0 x 5 mm (Endosseous Recalled by...
The Issue: Product not approved for use in the US
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...
The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...
The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...
The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.