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. 2,503 recalls have been distributed to Wyoming in the last 12 months.
Showing 15321–15340 of 27,462 recalls
Recalled Item: Atellica Sample Handler Prime (SMN 11069001). The Atellica" Solution is...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baby Quasar Plus Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not...
The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quasar MD Plus Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not...
The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250/MEVION S250i Proton Beam Radiation therapy system Product Usage:...
The Issue: QFix has advised Mevion Medical Systems that they are identifying...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Neonatal Flow Sensor Cable used on devices CARESCAPE R860 Recalled by...
The Issue: The Neonatal Flow Sensor Cable may be missing the connector housing exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Recalled by Philips Medical Systems Gmbh, DMC Due to The...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...
The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...
The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Release 3 (Stitching Patient Support) 712025 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028 Recalled...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Rel.4 Upgrades (Stitching Patient Support) 712084 Recalled...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028 Recalled...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to Gantry rotation or...
The Issue: Gantry rotation or proton irradiation can be allowed even if apertures or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Single Detector (Stitching Patient Support) 712020 Recalled...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028 Recalled...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Release 3 (Stitching Patient Support) 712025 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.