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. 2,526 recalls have been distributed to Wyoming in the last 12 months.
Showing 11981–12000 of 27,462 recalls
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific released a new Software Update Application that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imager II 5F Angiographic Catheters Recalled by Boston Scientific...
The Issue: Potential for tip detachment of Imager II 5F Angiographic Catheters
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intellijoint Navigation System Recalled by Intellijoint Surgical, Inc. Due...
The Issue: During total knee arthroplasty (TKA), the software may incorrectly calculate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology ECG Management Recalled by CHANGE HEALTHCARE CANADA...
The Issue: Inaccurate estimation of the heart rate may occur in instances where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Stick Sponge Presaturated W/PVP DYND70288H 2/PK Expiration Recalled...
The Issue: Voids were discovered in the packaging seal and loss of sterility on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Sterile 3mL Syringes with 21GA x 1 Inch Needle Recalled by Medline...
The Issue: Voids were discovered in the packaging seal and loss of sterility on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Winged Sponges Presaturated W/PVP DYND70289H Expiration 06/30/2022....
The Issue: Voids were discovered in the packaging seal and loss of sterility on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA Digital Radiography X- Ray system DR 800 with TomoSynthesis- Recalled...
The Issue: Tomosynthesis image acquisition sequence did not stop automatically after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ysio Recalled by Siemens Medical Solutions USA, Inc Due to The Ysio system...
The Issue: The Ysio system may process incorrect internal values for the position of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge 88-Series-washer disinfectors intended for cleaning Recalled by...
The Issue: Potential leakage that may occur due to ruptured spot welds in the chamber,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kits containing Covidien Force TriVerse Electrosurgical Devices. Distributed...
The Issue: Sterile packaging may potentially be compromised, and use of products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Force TriVerse Electrosurgical Devices Recalled by Covidien Llc Due...
The Issue: Sterile packaging may potentially be compromised, and use of products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuraGen Nerve Guide Recalled by Integra LifeSciences Corp. Due to...
The Issue: Nonconforming product which was dispositioned for rejection was mistakenly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys CA 19-9 Recalled by Roche Diagnostics Operations, Inc. Due to The...
The Issue: The firm has received an increased number of complaints concerning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems E2 Estradiol Catalog #: US: L2KE22(D) (200 Recalled by...
The Issue: Due to high discordant Estradiol results which.potentially affects all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and Recalled by...
The Issue: Due to high discordant Estradiol results which.potentially affects all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMO-7 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc....
The Issue: Complaints that the handle and/or activation knob on Hemostat devices have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMO-10 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc....
The Issue: Complaints that the handle and/or activation knob on Hemostat devices have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VNS Therapy Programmer Recalled by LivaNova USA Inc Due to False positive...
The Issue: False positive warning may occur after: 1) VNS Generator interrogated at 0mA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris System Recalled by CareFusion 303, Inc. Due to 1)Error...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.