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. 2,526 recalls have been distributed to Wyoming in the last 12 months.
Showing 12021–12040 of 27,462 recalls
Recalled Item: JOURNEY II UNI RESECTION PREP TRIAL Recalled by Smith & Nephew, Inc. Due to...
The Issue: The spike rail was manufactured with an oversized thru-hole which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pedicle Screws Recalled by Medicrea International Due to An internal...
The Issue: An internal component was assembled in the incorrect orientation, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAGEN Rotor Gene Q Software version 2.3.4. Real-time PCR analyzer Recalled...
The Issue: When using the Rotor-Gene Q with Software version 2.3.4 completing a LIMs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iliac Screws Recalled by Medicrea International Due to An internal component...
The Issue: An internal component was assembled in the incorrect orientation, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGRATH X3 Disposable Laryngoscope Blades-used with the McGRATH MAC Video...
The Issue: Blades do not fit the McGRATH MAC video laryngoscope handle or were tight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protective Cover Vivo 55/65 (Used for Vivo 50/65) Recalled by Breas Medical,...
The Issue: The outlet hole of the exhalation valve control pressure tube on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Truliant Splined Stem Extension Recalled by Exactech, Inc. Due to These...
The Issue: These Truliant Splined Stem Extension, 18mm x 120mm were found to have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: fridababy SmileFrida the TOOTHHUGGER 18+ months Triple Angle Brush Cleans...
The Issue: FridaBaby has been made aware through customer reports that the product is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREVI Isola Insrument and PREVI Isola Printer spares PSUs (power supply...
The Issue: The recall has been initiated due to potential for overheating or a fire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LN 3R70-01 Recalled by Abbott Gmbh & Co. KG Due to Abbott has identified...
The Issue: Abbott has identified potential performance issues for the Alinity ci...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Pheno-Interventional Fluoroscopic X-Ray System Model Number: 10849000...
The Issue: Potential exists for one or more axes of the robotic stand to become blocked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triton Canister System (finished part numbers FG 12009 Recalled by Stryker...
The Issue: Some Canister Scanning Labels used to calibrate the Triton Canister System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to There is an...
The Issue: There is an increased risk of false positive Proteus results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to There is an...
The Issue: There is an increased risk of false positive Proteus results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Braemar Manufacturing LLC DL950 Holter Monitor 1285 Corporate Center Dr....
The Issue: An issue with the DL900 and DL950 Series Holter Recorder was recognized on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Braemar Manufacturing LLC DL900 Holter Monitor 1285 Corporate Center Dr....
The Issue: An issue with the DL900 and DL950 Series Holter Recorder was recognized on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Columbus R/PS TIB.PLATEAU Cemented Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COLUMBUS CRA/PSA TIB.PLAT.CEMENTED Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COLUMBUS CR/PS TIB.PLAT.PLASMAPORE Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AS COLUMBUS CR/PS TIB.PLAT.CEMENTED Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.