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. 2,461 recalls have been distributed to Wyoming in the last 12 months.
Showing 19021–19040 of 27,462 recalls
Recalled Item: CPX4 Breast Tissue Expander 650 cc : Product Usage: Tissue Recalled by...
The Issue: The CPX4 Tissue Expander may have been packaged in the Artoura Tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ddR Formula B X-ray System Recalled by Swissray Medical Due to Possible...
The Issue: Possible injury due to movement of the arm, calibration loss and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit with Sharps Safety Features Permits access...
The Issue: Shipping carton labeling error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Module Model 8110 with software version 9.15 The Recalled by...
The Issue: A software anomaly with the Alaris Syringe module software version 9.15 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Line Catheterization Kit with Sharps Safety Features Permits access...
The Issue: Shipping carton labeling error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 23 G x .75 in. BD Vacutainer¿ Push Button Recalled by Becton Dickinson &...
The Issue: BD has received multiple reports of units associated with the 23 G x .75 in....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Calibrator U Recalled by Siemens Healthcare...
The Issue: Failure of analytical sensitivity with Calibrator U kit lots ending in 63...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nylon Surgical Suture for human use and vet use Recalled by Riverpoint...
The Issue: Nylon Surgical Sutures are recalled because the seals may become open during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polypropylene Surgical Sutures Recalled by Riverpoint Medical, LLC Due to...
The Issue: Polypropylene Surgical Sutures are recalled because the seals may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via picture archiving and communication system Syngo via is a Recalled...
The Issue: Software error. Incorrect values for the volume calculation from a freehand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: e.cam and Symbia E gamma camera systems with patient beds Recalled by...
The Issue: "We have received reports of patients hair being caught in the e.cam and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.x picture archiving and communication system Syngo.x is a software...
The Issue: Software error. Incorrect values for the volume calculation from a freehand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareLink iPro Version 1.10 Recalled by Medtronic Inc. Due to Medtronic...
The Issue: Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System Recalled by...
The Issue: Beckman Coulter is recalling the UniCel DxH Slidemaker Stainer Coulter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MISAGO RX Self Expanding Peripheral Stem Recalled by Terumo Medical Corp Due...
The Issue: During recent routine testing, the MISAGO Peripheral Stent was found not to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARDIA¿ 60cc Piston Irrigation Syringe Recalled by C.R. Bard, Inc. Due to...
The Issue: Package Defect: Products may be at risk for having a slit defect on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD¿ 70cc Piston Syringe with Catheter Tip Recalled by C.R. Bard, Inc. Due...
The Issue: Package Defect: Products may be at risk for having a slit defect on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD¿ Irrigation Recalled by C.R. Bard, Inc. Due to Package Defect: Products...
The Issue: Package Defect: Products may be at risk for having a slit defect on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome Recalled by LeMaitre Vascular, Inc. Due to...
The Issue: Wire which deploys the loop may be come detached at the handle causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD¿ Piston Syringe Recalled by C.R. Bard, Inc. Due to Package Defect:...
The Issue: Package Defect: Products may be at risk for having a slit defect on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.