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. 2,573 recalls have been distributed to Wyoming in the last 12 months.
Showing 701–720 of 27,462 recalls
Recalled Item: IntelePACS - InteleConnect / TechPortal Recalled by INTELERAD MEDICAL...
The Issue: Software application that receives digital images and data to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris infusion Pump Module 8100 Recalled by CareFusion 303, Inc. Due to...
The Issue: If infusion pump is dropped or severely jarred this may damage the pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem ID-B. Model/Catalog Number: SR103B Intended for use as an Recalled...
The Issue: Potential of negative recovery of the HBsAg analyte across two (2) lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem ID-B. Model Number: SR103B. Intended for use as an Recalled by...
The Issue: Potential of negative recovery of the HBsAg analyte across two (2) lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed...
The Issue: Due to an issue (potential breakage) with the shaft for the mounting of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BECKMAN COULTER BICARBONATE OSR6237 OSR6637 OSR6x37 Bicarbonate is Recalled...
The Issue: Bicarbonate reagent may generate falsely high Bicarbonate results due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EVIS EXERA III Duodenovideoscope Product Name: Olympus TJF-Q190V...
The Issue: Continued reports of positive cultures and infections have identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Luer Tip Caps Recalled by Becton Dickinson & Company Due to BD has...
The Issue: BD has confirmed through internal testing that certain device trays failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRI LED Mobile Exam Light Battery This non-magnetic Recalled by MRIMed Inc....
The Issue: Due to battery component overheating while charging resulting in melting of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phantom Fibula Nail Recalled by Paragon 28, Inc. Due to Fibula nail system...
The Issue: Fibula nail system intended for use in fixation of fibular fractures and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CentriMag Blood Pump Recalled by Thoratec LLC Due to Acute circulatory...
The Issue: Acute circulatory support system pump may not fit into the motor and reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DYNJ909119G ROBOTIC GASTRIC LAP SLEEVE-LF DYNJ909127F CYSTO DYNJ909129D...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.