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. 2,374 recalls have been distributed to Alaska in the last 12 months.
Showing 19201–19220 of 27,254 recalls
Recalled Item: TCA Board Recalled by Carefusion 211 Inc dba Carefusion Due to CareFusion...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA Standard with Compressor ventilator- Recalled by Carefusion 211 Inc dba...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA GDE/UIM upgrade kit Recalled by Carefusion 211 Inc dba Carefusion Due...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA Standard ventilator Recalled by Carefusion 211 Inc dba Carefusion Due...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dome Centric component ( 01.04227.005) from the Anatomical Shoulder (AS)...
The Issue: In some cases it has been difficult or not possible to disassemble the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Laboratory Automation System Recalled by Ortho-Clinical Diagnostics...
The Issue: If the user selects the Comment or Interpretation option (in the enGEN .gsb...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexichamber Anti-Static Valved Collapsible Holding Chamber Recalled by FSC...
The Issue: Product had torn/loose seal around the mouthpiece.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...
The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC Unit Model 8015 with software versions 9.17 and 9.19...
The Issue: A patient weight can be populated incorrectly under certain conditions when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...
The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...
The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norian Drillable Inject 5 CC-Sterile Recalled by Synthes (USA) Products LLC...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norian Drillable Inject 3 CC-Sterile Recalled by Synthes (USA) Products LLC...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Trabecular Metal Tibia Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Zimmer Inc. is initiating a recall of specific Persona" Trabecular Metal"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hettich Centrifuge Modules: StreamLAB Centrifuge Module (10372372 or...
The Issue: Premature bucket failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norian Drillable Inject 10 CC-Sterile Recalled by Synthes (USA) Products LLC...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Revolution CT The system is intended for head Recalled by GE Healthcare,...
The Issue: GEHC has become aware of a potential safety issue in the Revolution CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Histoplasma Yeast Complement Fixation Antigen Dilute Ref# H30150 The fungal...
The Issue: The device was found to have bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products AFP Reagent Pack Recalled by ORTHO-CLINICAL...
The Issue: Ortho Clinical Diagnostics (OCD) confirmed that specific lots of VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The System 83 Plus Recalled by Custom Ultrasonics, Inc. Due to To warn...
The Issue: To warn customers that Custom Ultrasonics, Inc. System 83 Plus AERs should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.