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. 2,510 recalls have been distributed to Wyoming in the last 12 months.
Showing 12481–12500 of 27,462 recalls
Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...
The Issue: The products may have been packaged with an incorrect Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haylard Closed Suction System for Neonates/Pediatrics Recalled by Avanos...
The Issue: Avanos Medical has received reports stating that the central lumen of some 5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinias DAP Meter Recalled by Shimadzu Medical Systems Due to The DAP meters...
The Issue: The DAP meters were found to be outside of tolerance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Histoplasma Immunodiffusion (ID) Antigen Recalled by Immuno-Mycologics, Inc...
The Issue: False positive results due to potential contamination of reagent.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medacta Shoulder SYSTEM HUMERAL ANATOMICAL METAPHYSIS Recalled by Medacta...
The Issue: Certain lot numbers of the Medacta Humeral Anatomical Cementless Metaphysis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Juno DRF Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to...
The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo EZ Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to...
The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo DRF Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to...
The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to the...
The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ascension¿ Silicone PIP-Silicone PIP Sz 1 Recalled by Integra Lifesciences...
The Issue: Silicone PIP Implant mislabeled as a size 1 implant on the outer packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Site~Rite 8 Ultrasound Systems-intended for diagnostic ultrasound imaging of...
The Issue: The indicator may show available charge when the battery is close to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 ANA Screen Control Set Recalled by Bio-Rad Laboratories, Inc....
The Issue: A new lot of ANA screen control and any subsequent control lots are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube - Product Recalled by...
The Issue: The tracheal and brochial swivel connectors are incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oral-B Recalled by Young Dental Manufacturing Co, LLC Due to Product shelf...
The Issue: Product shelf life may be shorter than that indicated on the label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XEN Gel Stent Recalled by Allergan PLC Due to Foreign Object Contamination
The Issue: Residual polishing compounds, that are used in the needle sleeve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroDot brand: Wave Prep 4 oz. tubes-Product 1710-03. An electroconductive...
The Issue: Product has the potential to be contaminated with Burkholderia cepacia (B....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroDot brand: Wave Prep Single use cups Recalled by Bio-Signal Group Corp....
The Issue: Product has the potential to be contaminated with Burkholderia cepacia (B....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius 2 Tympanic Thermometer OEM Tympanic Item Code:303062 Recalled by...
The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius 2 Tympanic Thermometer Private Label Item Code: 3069 Recalled by...
The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius 2 Tympanic Thermometer (discontinued) Item Code: 303000 Recalled by...
The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.