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. 2,404 recalls have been distributed to Wyoming in the last 12 months.
Showing 22741–22760 of 27,462 recalls
Recalled Item: Accusorb MRI MAC7004 Part Number: MRI-04 MRI-Poncho Product Usage: Radio...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7006 Part Number: MRI-06 MRI-Large Torso Wrap Product...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7009 Part Number: MRI-09 MRI- Leg Wrap Blanket Recalled by...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7007 Part Number: MRI-07 MRI-Breast Shield Product Usage:...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7030 Product Usage: Radio frequency shielding blankets and...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Avalon Monitors with software revision J.30.58: Model Product FM20...
The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Monitors with software revisions J.21.03 Recalled by...
The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural Knee II Revision Femoral Stem Recalled by Zimmer, Inc. Due to Failed...
The Issue: Failed to meet established requirements for sterile barrier integrity due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Recalled...
The Issue: A recall of the APTUS Ulna Shortening 2.5 instrument was initiated due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transport Rollator with Padded Seat Recalled by Roscoe Medical Inc Due to...
The Issue: The caster may separate completely from the device frame causing injury to user.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Puritan Bennett 980 Ventilator Recalled by Nellcor Puritan Bennett...
The Issue: Covidien is recalling certain Puritan Bennett 980 Ventilator Systems due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spline Twist Implant Recalled by Zimmer Dental Inc Due to Zimmer Dental is...
The Issue: Zimmer Dental is recalling Tapered Screw-Vent Implants because the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered Screw-Vent Implant Recalled by Zimmer Dental Inc Due to Zimmer...
The Issue: Zimmer Dental is recalling Tapered Screw-Vent Implants because the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuum Acetabular System Trabecular Metal Shell with Multi Holes Recalled...
The Issue: The affected products are missing polar boss threads.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo SET uSpO2 Cable The Masimo SET uSpO2 Pulse Oximetry Recalled by...
The Issue: Firm has identified a small number of Oximetry Cables with crossed-internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension HB1C Flex reagent cartridge Recalled by Siemens Healthcare...
The Issue: Certain lots of the reagent cartridges show confirmed positive bias...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symmetric Total Knee Femoral Components Product Usage: Symmetric Total Knee...
The Issue: Packaging of a device was compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Healthcare Recalled by Merge Healthcare, Inc. Due to It has been...
The Issue: It has been reported that during use, the SpO2 value displayed on the Hemo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD-Solis Medication Safety Software Recalled by Smiths Medical ASD, Inc....
The Issue: Smiths Medical has identified an issue with a single batch (Lot Number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coloplast Conveen Urine Collection Leg Bag Recalled by Coloplast...
The Issue: Coloplast is recalling the Conveen Contour Leg Bag due to potential leakage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.