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 22441–22460 of 27,254 recalls
Recalled Item: Fisher and Paykel Healthcare (FPH) IW900-Series Infant Warmer Fisher and...
The Issue: Breakage of the nut that secures the heater head in place, which can cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONMED ADULT R2 Multifunction Electrodes Recalled by ConMed Corporation Due...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONMED PEDIATRIC R2 Multifunction Electrodes Recalled by ConMed Corporation...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI PEDIATRIC Radiotransparent Electrode Recalled by ConMed Corporation Due...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polyflux Revaclear Max Dialyzer Recalled by Gambro Renal Products Inc Due to...
The Issue: Gambro is initiating a field action for Polyflux Revaclear Dialyzer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Function Analysis Software Product Data No. MPDCT0301EAD CSCF-003A...
The Issue: Potential problem with the cardiac function analysis software (CFA)....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ 5 Ultrasound System Recalled by Philips Ultrasound, Inc. Due to When...
The Issue: When using the QLAB Auto 2D Quantification (a2DQ) and Auto Cardiac Motion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q-Station Quantification Software. Q-Station 3.0 with a2DQ and/or aCMQ...
The Issue: When using the QLAB Auto 2D Quantification (a2DQ) and Auto Cardiac Motion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Function Analysis Software Product Data No. MPDCT0301EAD CSCF-003A...
The Issue: Potential problem with the cardiac function analysis software (CFA)....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polyflux Revaclear Dialyzer Recalled by Gambro Renal Products Inc Due to...
The Issue: Gambro is initiating a field action for Polyflux Revaclear Dialyzer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ 7 Ultrasound System Recalled by Philips Ultrasound, Inc. Due to When...
The Issue: When using the QLAB Auto 2D Quantification (a2DQ) and Auto Cardiac Motion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Additional devices identified in new FSN MA-FCO 83000190: QLAB versions...
The Issue: When using the QLAB Auto 2D Quantification (a2DQ) and Auto Cardiac Motion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pulsiocath PiCCO ProAQT Monitoring Kit Recalled by Pulsion Medical Inc Due...
The Issue: Internal testing and investigation of the packaging revealed cracks and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile drape Recalled by Novadaq Technologies, Inc. Due to Mislabeling
The Issue: Non sterile-drape LUNA drape was inadvertently mislabeled with an additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...
The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...
The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGrath MAC2 Video Laryngoscope Blades Product supplied in box of 50 items...
The Issue: The blade retaining clip may be difficult to engage and thereby increase the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUNA Chest Recalled by Novadaq Technologies, Inc. Due to Mislabeling
The Issue: Non sterile-drape LUNA drape was inadvertently mislabeled with an additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Silhouette and/or MiniMed Sure-T Infusion Sets Recalled by...
The Issue: Tubing may detach at the connect/disconnect location on the MiniMed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...
The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.