Product Recalls in Idaho
Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,395 recalls have been distributed to Idaho in the last 12 months.
Showing 26661–26680 of 27,833 recalls
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ILLlCO¿ MIS Posterior Fixation System Recalled by Alphatec Spine, Inc. Due...
The Issue: The firm initiated the recall because the stainless steel guide-wire of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hem-o-lok Large Polymer Ligating Clips Recalled by Teleflex Medical Due to...
The Issue: Product is being recalled due to the possibility that the tray may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (l) Visum Halogen Surgical Light Recalled by Stryker Communications, Inc....
The Issue: Stryker has become aware that there is a low likelihood of incomplete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cozy Comfort Premier Recliner 5580 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER CARE RECLINER 5570/5574 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Designer Care Cliner 6700/6704/6710 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray V12 Size: 320 mm X 320 mm X 450 Recalled by Mindray DS USA, Inc....
The Issue: Mindray has identified an issue with the V Series Monitor where the monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER LIFECARE RECLINER 5400 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Centrifugal System Control module System 9000 The Sarns Centrifugal...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Centrifugal System Control module Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Centrifugal System Control module Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog...
The Issue: We are notifying you of a potential interaction between therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIA Radiation Oncology Recalled by Varian Medical Systems, Inc. Oncology...
The Issue: An anomaly has been identified with the ARIA Oncology Information System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CapLOX II Final Torque Driver Recalled by Captiva Spine, Inc Due to Captiva...
The Issue: Captiva Spine recalled their CapLOX II Final Torque Driver, Indicator due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Flow Module indicated for use Recalled by...
The Issue: Terumo Cardiovascular Systems (CVS) received one report of a flow module for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 220amx Mobile general purpose radiographic imaging...
The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCP Pump Control Panel Recalled by Sorin Group USA, Inc. Due to Sorin Group...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCP Pump Control Panel Recalled by Sorin Group USA, Inc. Due to Sorin Group...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.