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. 2,573 recalls have been distributed to Wyoming in the last 12 months.
Showing 1741–1760 of 27,462 recalls
Recalled Item: Atellica IM Homocysteine Calibrator (2 Pack). Siemens Material Number:...
The Issue: Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...
The Issue: Patient Monitor software update to address issues:1)May freeze at startup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur HCY Calibrator (2 Pack). Siemens Material Number: 10310376....
The Issue: Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CRP Slides. One sales unit contains 5 cartridges...
The Issue: Product was incorrectly assigned GEN 88 instead of GEN 83 on product carton,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " Recalled by Prismatik...
The Issue: Due to packaging mix up. Package of finished devices were reported to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Augmedics Perc Pin Adaptor Recalled by Augmedics Ltd. Due to The perc pin...
The Issue: The perc pin adaptor AMCH07200 tightening knob was found to be inconvenient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plus Initial Drill Recalled by Straumann USA LLC Due to The batch was...
The Issue: The batch was produced without the laser engraving of 7 mm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TufTex Over-the-Wire Embolectomy Catheter. All Catalog numbers: 1651-34...
The Issue: During internal product testing, it was observed that some packages to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pruitt Occlusion Catheter. Catalog Numbers: 2103-36 Recalled by LeMaitre...
The Issue: During internal product testing, it was observed that some packages to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X)...
The Issue: Potential for the presence of visible foreign matter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN Craniotomy Kit Recalled by Integra LifeSciences Corp. (NeuroSciences)...
The Issue: Inadequate weld that can potentially cause the product to disassemble.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Recalled by Medical...
The Issue: Potential for DC Power Supply housing to become hot to the touch and deform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09 Recalled by...
The Issue: During internal product testing, it was observed that some packages to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN Disposable Perforator Recalled by Integra LifeSciences Corp....
The Issue: Inadequate weld that can potentially cause the product to disassemble.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CMS8000 Patient Monitor Recalled by Contec Medical Systems Co., Ltd. Due to...
The Issue: Patient monitor has nine identified cybersecurity vulnerabilities.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit...
The Issue: Adapters may disconnect during setup or while in use, potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Solis VIP Ambulatory Infusion Pump Models: 1) PUMP KIT Recalled by...
The Issue: There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit...
The Issue: Adapters may disconnect during setup or while in use, potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD-Solis HPCA Ambulatory Infusion Pump Recalled by Smiths Medical ASD,...
The Issue: Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD-Solis VIP Ambulatory Infusion Pump Recalled by Smiths Medical ASD, Inc....
The Issue: Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.