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 14001–14020 of 27,462 recalls
Recalled Item: EV1000 Clinical Platform Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Potential for an electrical short circuit leading to possible fire hazard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System 10 MM Recalled by Conmed Corporation...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System 15 MM Recalled by Conmed Corporation...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System" Recalled by Conmed Corporation Due to...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via syngo.CT Cardiac Function Recalled by Siemens Medical Solutions...
The Issue: There is a potential risk of a wrong measurement in the annulus plane during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via syngo.CT Cardiac Planning Recalled by Siemens Medical Solutions...
The Issue: There is a potential risk of a wrong measurement in the annulus plane during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics Due...
The Issue: Potential for sample fluid to be dispensed to an incorrect position on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Digital Linear Accelerators of type: ARTISTE MV System MEVATRON...
The Issue: Advisory issued not to disable or bypass the AMP function. Disabling or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Servo-I Ventilator System -EDI CATHETER PHT Free 6Fr/49cm 5/pkg...
The Issue: Edi Catheter labeled with wrong expiry date on single pack EDI catheter boxes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIR Technology Anterior Array Recalled by GE Healthcare, LLC Due to The...
The Issue: The outer seam of the coil, closest to the system cable, may separate and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neomem Resorbable Collagen Membrane Recalled by Collagen Matrix, Inc. Due to...
The Issue: Product was packaged in the wrong box; may have been placed inside a Neomem...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OnSight 3D Extremity System- X-Ray Recalled by Carestream Health, Inc. Due...
The Issue: When the user performs the re-assignment of a parent / companion pair, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Performance Series Sagittal Blade Recalled by Stryker Instruments Div. of...
The Issue: During manufacture, packaging materials for a small portion of the lot may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDEAL IMPLANT Structured Breast Implant Recalled by Ideal Implant...
The Issue: The implants were deflating due to a piece of silicone disrupting the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to Continuous...
The Issue: Continuous operation at very high tube output may result in increased wear...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Albumin BCP Product Usage: ALBP is an in vitro test Recalled by Roche...
The Issue: The reagent lot is exhibiting calibration failures, QC imprecision, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Laboratories Ltd. Catalogue Number CQ5052 Recalled by Response...
The Issue: The form received three complaints related to the user obtaining a result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.