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. 2,484 recalls have been distributed to Wyoming in the last 12 months.
Showing 15421–15440 of 27,462 recalls
Recalled Item: VOLISTA StandOP Surgical Light Recalled by Maquet SAS Due to Certain VOLISTA...
The Issue: Certain VOLISTA StandOP Surgical Lights have been identified as having a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arctic Sun Temperature Management System Recalled by Bard Medical Division...
The Issue: An improper wiring connection on the chiller assembly may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-SPOT Recalled by Beekley Corporation Due to There is a potential for...
The Issue: There is a potential for imaging artifact to mimic calcifications on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY BCS OXINIUM Knee Femoral Components Recalled by Smith & Nephew, Inc....
The Issue: The data in the National Joint Registry of England, Wales and Northern...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY BCS Knee Conventional Polyethylene Inserts: 74023111 Recalled by...
The Issue: The data in the National Joint Registry of England, Wales and Northern...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoSPOT Recalled by Beekley Corporation Due to There is a potential for...
The Issue: There is a potential for imaging artifact to mimic calcifications on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Biosystems HistoCore SPECTRA ST Recalled by Leica Microsystems, Inc....
The Issue: These devices have an incorrect specification against safety standard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Journey BCS Knee CoCr Femoral Components Recalled by Smith & Nephew, Inc....
The Issue: The data in the National Joint Registry of England, Wales and Northern...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-SPOT Recalled by Beekley Corporation Due to There is a potential for...
The Issue: There is a potential for imaging artifact to mimic calcifications on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2" Recalled by Teleflex...
The Issue: The incorrect plastic was used to manufacture the handles of these shears,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspire II Model 3024 Implantable Pulse Generator (IPG) for Obstructive...
The Issue: Incorrect use-by date on the device registration/patient file labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy 100 Recalled by Philips Respironics, Inc. Due to In 2018, Philips...
The Issue: In 2018, Philips Respironics added foam replacement to the preventive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Alpha Recalled by ESAOTE S.P.A. Due to The probe power monitoring...
The Issue: The probe power monitoring settings have been found to be not appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centron Product Usage: Vascular Recalled by Philips Healthcare Due to The...
The Issue: The first time an operator selects a new procedure type during a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Express Fluid Warmer (FW-300 Recalled by NxStage Medical, Inc. Due...
The Issue: There is a potential risk of electrical fire when fluid leaks into the power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nokia BPM+ Wireless Blood Pressure Monitor Product System Recalled by...
The Issue: Device could not meet the requirements for systolic pressure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.