Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,383 recalls have been distributed to Wyoming in the last 12 months.
Showing 24181–24200 of 27,462 recalls
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Intermittent noise on...
The Issue: Intermittent noise on ECG and/or Respiration waveforms associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Recalled by...
The Issue: The recalling firm determined that visual inspections of the fork joints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S5/C5 Heart-lung machine Product Usage: The StOckert S5/ Sorin C5 Recalled...
The Issue: Sorin is initiating a field correction on S5/C5 Heart-lung machine and CP5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CP5 centrifugal pump system Product Usage: The Stockert S5/ Sorin Recalled...
The Issue: Sorin is initiating a field correction on S5/C5 Heart-lung machine and CP5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invivo Corporation Expression Information Portal (Model IP5) is intended to...
The Issue: Invivo Corporation located at 12151 Research Parkway, Orlando, FL 32826 is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System (Brilliance CT Big Bore Oncology & Recalled...
The Issue: Machine Name in TumorLOC Basic Mode is obscured. When TumorLOC is in Basic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABACUS TPN Calculation Software Recalled by Baxter Corporation Englewood Due...
The Issue: Baxter Healthcare Corporation is issuing a voluntary correction for ABACUS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anspach Irrigation Clip 40 Product Usage: Irrigation clips provide a...
The Issue: The Irrigation Clips were assembled with the incorrect (smaller) clips.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAS Omni Immune PRO Controls Recalled by Microgenics Corporation Due to The...
The Issue: The constituent, Inhibin A, was removed from MAS Omni IMMUNE and MAS Omni...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAS Omni Immune Controls Recalled by Microgenics Corporation Due to The...
The Issue: The constituent, Inhibin A, was removed from MAS Omni IMMUNE and MAS Omni...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: steroEOS Workstation with software versions: 1.3 Recalled by EOS Imaging Due...
The Issue: Error copying information to the clinical file and to the report when two 3D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carescape Patient Data Module The Patient Data Module Recalled...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: outer box: Recalled by Biomet, Inc. Due to Inner label of PN: 906768 Lot:...
The Issue: Inner label of PN: 906768 Lot: 055450 CurvTek Eye Needle 22mm X-Large states...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Camino Advanced Monitor with Waveform Display Model CAM01 Integra...
The Issue: Integra became aware through a complaint from a single non-US customer that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InstaTrak¿ 3500 Plus Recalled by GE OEC Medical Systems, Inc Due to GE OEC...
The Issue: GE OEC Medical Systems Inc is recalling InstaTrak¿ 3500 Plus, ENTrakTM Plus,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular Screw 6.5mmx35mm Part Number: 010001000 Recalled by Biomet,...
The Issue: Investigation identified that the outer label, inner label, and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra LifeSciences is voluntarily recalling any unexpired lots of HITHSP10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Interlink threaded lock cannula This is a locking blunt Recalled by...
The Issue: BD Interlink Threaded Lock Cannula REF# 303369 and lot #3021392 is being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthofix Firebird Spinal Fixation System Instrumentation Modular Screw...
The Issue: Orthofix received 6 complaints which resulted in a reportable events due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.