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. 2,245 recalls have been distributed to Alaska in the last 12 months.
Showing 45481–45500 of 46,762 recalls
Recalled Item: Aesculap SIBD 4 degree Trial Implant (SJ768T-US) and Aesculap SIBD Recalled...
The Issue: The 4 degree and 9 degree trial instruments (SJ768T-US/SJ780T-US) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Transdermal System Recalled by Actavis Due to Subpotent; some...
The Issue: Subpotent; some patches may not contain fentanyl gel
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Safe Spot Infant Resuscitator Recalled by Ventlab Corporation Due to...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe Spot Infant Resuscitator Recalled by Ventlab Corporation Due to...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFlow Resuscitator Recalled by Ventlab Corporation Due to Possible volume...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V*Care Resuscitator Infant Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Resuscitator Recalled by Ventlab Corporation Due to Possible volume...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Rescue Med Infant Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFlow Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breath Tech Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFlow Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Premium Small Child Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stat-Check Resuscitator Recalled by Ventlab Corporation Due to Possible...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Premium Small Adult Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MultiDiagnost Eleva with Flat Detector (MD Eleva FD)Model: 708034...
The Issue: When doing a 3 Dimensional Rotational Angiography (3DRA) the 3D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Narrow CrossFit (NC) Screw for CARES Abutment ZrO2. Endosseous...
The Issue: Incorrect Screw (RC) included with NC CARES Abutment Set was not a Narrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima XR220amx Mobile general purpose radiographic imaging of the human...
The Issue: Software issue: a violation of 21 CFR 1020.31(a). After an image is taken,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima XR200amx. Mobile general purpose radiographic imaging of the human...
The Issue: Software issue: a violation of 21 CFR 1020.31(a). After an image is taken,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chromovision High Definition (HD) Wireless Camera Recalled by Berchtold...
The Issue: Defective camera: There is a possibility that the connection of the wires to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX CV Reporting The Results Management (RM)/IMPAX CV reporting component...
The Issue: When users selected "Left stenosis" in the "Graft Duplex Conclusion" section...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.