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. 2,535 recalls have been distributed to Wyoming in the last 12 months.
Showing 8621–8640 of 27,462 recalls
Recalled Item: BALLARD* Multi-Access Port Catheter Recalled by Avanos Medical, Inc. Due to...
The Issue: Product was distributed with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALLARD* Multi-Access Port (MAP) Catheter Recalled by Avanos Medical, Inc....
The Issue: Product was distributed with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALLARD* Seal Cassette Replacement MAP - BALLARD* Seal Cassette Replacement...
The Issue: Product was distributed with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack Recalled...
The Issue: Lower than expected results for VITROS¿ Immunodiagnostic Products TSH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electri-Cool II Portable Cold Therapy Unit Recalled by Gentherm Medical, LLC...
The Issue: This recall has been initiated to provide a labeling update with revised...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar) Recalled by...
The Issue: The U-channel sheaths may cause damage to ProACT implant devices when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Edge Plus-Computed tomography system Model 1026700 Recalled by...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS-Computed tomography system Model 8098027 Recalled by...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge -Computed tomography system Model 10590000 Recalled...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Confidence -Computed tomography systems Model 10590100 Recalled by...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use for all model numbers of the Medtronic Recalled by...
The Issue: There have been reports of stent migration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper FD series with Software Version Number: 2.1.x- Recalled...
The Issue: Set screws securing the two gliding rods of the Extra Monitors (called 7th...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer with Software version: V1.25.1 and lower- An...
The Issue: (1)Software (SW) versions V1.25.1 and lower may result in TDef (Test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES HSV 1&2 Assay Recalled by Luminex Corporation Due to Impacted lot may...
The Issue: Impacted lot may leak inside the ARIES instrument. Testing confirmed a leak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Senior Living Arial Emergency and Nurse Call Systems Recalled by Stanley...
The Issue: Systems are not alarming due to increased memory consumption.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas LiatSystem Recalled by Roche Molecular Systems, Inc. Due to Roche has...
The Issue: Roche has identified a small number of cobas Liat analyzer units that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instavac Portable Suction Pump Recalled by Ohio Medical Corporation Due to...
The Issue: Increase in premature device failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultimum HEMOSTASIS INTRODUCER 5f 1.67 MM Recalled by Abbott Due to As a...
The Issue: As a result of a manufacturing error, one (1) lot of Ultimum Hemostasis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-75...
The Issue: Firm is initiating a correction due to the possibility of fluid ingress....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-31...
The Issue: Firm is initiating a correction due to the possibility of fluid ingress....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.