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. 2,484 recalls have been distributed to Wyoming in the last 12 months.
Showing 16841–16860 of 27,462 recalls
Recalled Item: 3.0 mm Reaming Rod Recalled by Synthes (USA) Products LLC Due to Possible...
The Issue: Possible lack of product sterility due to potential gaps/channeling in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Imaging version V31 (model # 10014063) is a Picture Recalled by...
The Issue: Siemens is releasing a letter to inform about potential data loss relevant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ArrowADVANTAGE 5 Pressure Injectable Peripherally Inserted Central Catheter...
The Issue: Finished good kits may contain incorrect components. Kits that should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW PICC powered by ARROW VPS Stylet Recalled by Arrow International Inc...
The Issue: Finished good kits may contain incorrect components. Kits that should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium VR 1210 Recalled by Sorin Group Italia SRL - CRF Due to There is a...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium CRT DF1 1711 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium CRT-D 1741 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium DR DF4 1540 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew POLARSTEM(TM) Femoral Stems with Ti/HA (Standard Recalled by...
The Issue: The Cardan joint of the Polarstem Cardan could potentially fracture or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium VR DF4 1240 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium DR 1510 Recalled by Sorin Group Italia SRL - CRF Due to There is a...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Direct Swish Duo-Grip Healing Collar Recalled by Implant Direct...
The Issue: The Swish Duo-Grip Healing Collar part number 9048-13H (4.8mm) package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FUJINON ED-530XT. This device is intended for the visualization of Recalled...
The Issue: An update to the design and labeling was implemented to help reduce patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sekisui Diagnostics Sekure Chemistry Acetaminophen L3K Recalled by Beckman...
The Issue: Reagent carryover from Sekisui ACTH when utilized on the BEC AU 680 analyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife(TM) Reduced Heparin ARTERIAL BLOOD SAMPLER Recalled by Vyaire...
The Issue: Lot #0001047501 of the 9025RHTR ABG sampling kits have been manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas 8000 Modular Analyzer Series Recalled by Roche Diagnostics Corporation...
The Issue: A warning is being added to the cobas¿ 6000 analyzer and the cobas¿ 8000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Elastic Esmark Bandage Recalled by Medline Industries Inc Due to...
The Issue: Product did not undergo correct sterilization procedures and may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas 6000 Modular Series system Recalled by Roche Diagnostics Corporation...
The Issue: A warning is being added to the cobas¿ 6000 MODULAR Series System - c501 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 100 Intra-Aortic Balloon Pump. It supports the heart's left Recalled by...
The Issue: False blood back detection alarm and the ingress of fluids into the IABP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Product Usage: is a software system designed for treatment...
The Issue: For the proton QA preparation module in RayStation 6 (including SP1 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.