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. 2,415 recalls have been distributed to Wyoming in the last 12 months.
Showing 19961–19980 of 27,462 recalls
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helioseal Clear 1 x 1.25 g Recalled by Ivoclar Vivadent, Inc. Due to...
The Issue: Complaints were received claiming the material failed to polymerize under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10mm X 12o Solitaire Ti Medium Spacer Solitaire Anterior Spinal System...
The Issue: Zimmer Biomet Spine initiated a recall of certain Solitaire Ti Spacers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD SurePathTM Preservative Collection Vials Recalled by Becton Dickinson &...
The Issue: BD has confirmed that a portion of BD SurePath" collection vials associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC Unit Recalled by CareFusion 303, Inc. Due to CareFusion is...
The Issue: CareFusion is recalling the Alaris PC unit because a component on the PC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instinct¿ Java¿ System (IFU : 046WAN0000T) . Stabilizes one or Recalled by...
The Issue: Zimmer Biomet is initiating a Medical Device Correction Notice to provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammomat Inspiration with Tomosynthesis functionality Recalled by Siemens...
The Issue: A potential system fatal error may occur during tomosynthesis reconstruction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Clamp¿ System (IFU : SNA027-N-90001). Provides the stability...
The Issue: Zimmer Biomet is initiating a Medical Device Correction Notice to provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Inform II Base Unit as a part of the Recalled by Roche Diagnostics...
The Issue: Accu-Chek Inform II Base Unit might produce physical transmission errors in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451...
The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Group A Strep Direct (MOL2850) with Direct Amplification Disc...
The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Flu A/B & RSV Direct (MOL2650) with Direct Amplification Disc...
The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eValueMed Infant Transport Mattress 301-1015 Recalled by Philips Electronics...
The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: evaluemed Infant Heel Warmer 301-1223 Recalled by Philips Electronics North...
The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightSpeed Ultra (8-slice MDAS) Recalled by GE Medical Systems, LLC Due to...
The Issue: GE Healthcare has updated the Service Manuals for a number of CT and PET CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery LS Recalled by GE Medical Systems, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has updated the Service Manuals for a number of CT and PET CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.