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. 2,480 recalls have been distributed to Alaska in the last 12 months.
Showing 14081–14100 of 27,254 recalls
Recalled Item: Spacelabs Healthcare Smart Disclosure System Recalled by Spacelabs...
The Issue: Several reports were received that patient records were printed with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kii Fios First Entry Recalled by Applied Medical Resources Corp Due to The...
The Issue: The product may not have met sterility requirements . Use of a non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON NX2 Elite Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: The action is being initiated due to internal testing which identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON NX3 Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: The action is being initiated due to internal testing which identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON NX3 Elite Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: The action is being initiated due to internal testing which identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON NX2 Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: The action is being initiated due to internal testing which identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fetal Spiral Electrode Recalled by Philips North America, LLC Due to During...
The Issue: During use of the Philips FSE, it is possible for the metal electrode tip to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Obturator (long cone) Recalled by Medrobotics Corporation Due to The weld...
The Issue: The weld may break, resulting in the rod separating from the cone of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Obturator (shortcone) Recalled by Medrobotics Corporation Due to The weld...
The Issue: The weld may break, resulting in the rod separating from the cone of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lithium-ion Rechargeable Batteries for the Philips MX40 Wearable Monitor by...
The Issue: Lithium-ion Rechargeable Batteries for the Philips MX4O Wearable Monitor may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PET Plates Coated Film-MONOMEDBV2S2- Radiographic Film Recalled by Agfa N.V....
The Issue: Due to an inhomogeneous coating solution, pinholes can become visible in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIUS Blower Mister Product Code/: CB-1000 The Axius Blower Recalled by...
The Issue: Potential lack of carbon dioxide (CO2) flow that may result in a procedural...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution CT scanners Product Usage: The system is intended for head...
The Issue: Additional low dose radiation exposure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SKINFUSE Resuce Calming Complex Kit containing: SKINFUSE LIFT HG - Recalled...
The Issue: Cosmetic Kit was packaged with a mislabel medical product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: On-X Aortic Heart Valve with Anatomic Sewing Ring Product Usage: Recalled by...
The Issue: On-X Valve was mislabeled with the incorrect serial number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences(R) IntraClude(TM) Intra-Aortic Occlusion Device is a...
The Issue: Edwards Lifesciences has received a limited number of customer reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipid Panel test strips (as a component of smart bundles) Recalled by...
The Issue: Some lots of test strips do not fit tightly into the optical block, and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CHOL+HDL+GLU test strips Recalled by Polymer Technology Systems, Inc. Due to...
The Issue: Some lots of test strips do not fit tightly into the optical block, and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipid Panel test strips Recalled by Polymer Technology Systems, Inc. Due to...
The Issue: Some lots of test strips do not fit tightly into the optical block, and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm FDR Go PLUS Recalled by Fujifilm Medical Systems U.S.A., Inc. Due...
The Issue: FUJIFILM Medical Systems U.S.A., Inc., Modality Systems became aware of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.