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. 2,535 recalls have been distributed to Wyoming in the last 12 months.
Showing 8181–8200 of 27,462 recalls
Recalled Item: BD Synapsys Microbiology Informatics Solution Recalled by Becton Dickinson &...
The Issue: When updating BD Kiestra customers to BD Synapsys version 4.10, the custom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RocheDiabetes Care Platform Software version 2.5.2 material number...
The Issue: Potential for patient data mismatch when using browser "back" button to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.0mm x 10mm Cannulated Screw Recalled by Acumed LLC Due to Cannulated...
The Issue: Cannulated Screws 4.0mm x 10mm and 4.0mm x 12mm may not have sufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.0mm x 12mm Cannulated Screw Recalled by Acumed LLC Due to Cannulated...
The Issue: Cannulated Screws 4.0mm x 10mm and 4.0mm x 12mm may not have sufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Standard PVC Laryngeal Masks Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The mask cuff may disconnect from the device's breathing tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-MP60: OES Bronchofiberscope Recalled by Olympus Corporation of the...
The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-3C160: EVIS EXERA Bronchovideoscope Recalled by Olympus Corporation of...
The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-MP160F: EVIS EXERA Bronchofibervideoscope Recalled by Olympus Corporation...
The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-1TQ180: EVIS EXERA II Bronchovideoscope Recalled by Olympus Corporation...
The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product Recalled by SIMPLIVIA...
The Issue: Disconnection of the OnGuard2 Bag Adaptor SP from infusion bags which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT STAT Myoglobin Calibrators Recalled by Abbott Laboratories Due to...
The Issue: This calibrator lot did not meet acceptance criteria during ongoing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acuson 9vE4 Transducer Recalled by Siemens Medical Solutions USA, Inc. Due...
The Issue: Transducers (component of ultrasound system) may exceed recommended thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...
The Issue: Upgraded software version makes an automatic change in laser configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on syngo.via Recalled by...
The Issue: Upgraded software version makes an automatic change in laser configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...
The Issue: Upgraded software version makes an automatic change in laser configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...
The Issue: Upgraded software version makes an automatic change in laser configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS SOMATOM with software syngo CT VA30A_SP4 Models: SOMATOM go.Now...
The Issue: Software error may result in sporadic problems causing scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YSIO X.Pree Recalled by Siemens Medical Solutions USA, Inc Due to For the...
The Issue: For the automated multi-image-acquisition procedure Ortho x-ray collimation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold)...
The Issue: The product was distributed without FDA authorization or clearance for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drager Infinity CentralStation Software versions VG2.1.2 and VG2.1.2 SU12....
The Issue: Software issue resulting in temporary loss of central monitoring functionality.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.