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. 2,378 recalls have been distributed to Wyoming in the last 12 months.
Showing 26581–26600 of 27,462 recalls
Recalled Item: Serial interface module RS-232 Product Usage: The System 1 provides Recalled...
The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interface module for CDl System 500 Product Usage: The Interface Recalled by...
The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart FRx 861304 Automated External Defibrillator Manufactured...
The Issue: Philips determined that it is important to clarify information in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon Mini - 3788 (IPG) Recalled by St. Jude Medical Due to As part of St....
The Issue: As part of St. Jude Medical's routine tracking and product monitoring, they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips and Laerdal brands of HeartStart HS1 Defibrillator Family Model...
The Issue: Philips determined that it is important to clarify information in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Styker Orthobiologics Vita Plasma Separator Recalled by Stryker...
The Issue: When preparing plasma using VitaPrep, it was reported that a small amount of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon - 3701 (Wall Charger) and 3711 (Portable Charger). Product Recalled by...
The Issue: St. Jude Medical has informed your doctor that a number of cases have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon Mini - 3721 (Charger). Product Usage: Eon Mini system Recalled by St....
The Issue: St. Jude Medical has informed your doctor that a number of cases have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Multi-Diluent 1 - Used for automated dilutions...
The Issue: Decrease in onboard dilution recovery when using Multi-Diluent 1 that has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap S4 Element 4.5mm Polyaxial Screws (ST240T Recalled by Aesculap...
The Issue: There is a possibility that the screw channel that holds the rod in place...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Folate Calibrators Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the Access Folate Calibrators because it may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capintec Captus 3000 Thyroid Uptake System Nuclear uptake probe intended...
The Issue: Customers who received a Capintec Captus 3000 Thyroid Uptake System with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Folate WHO Calibrators Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is recalling the Access Folate Calibrators because it may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Spine EXPEDIUM Offset Torque Wrench Product Code 2797-29-510 The...
The Issue: A component within the handle of the Expedium Offset Torque Wrench is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaTREK Windows Software Recalled by Trek Diagnostic Systems Due to Review...
The Issue: Review of instrument software databases and investigation of two customer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cisco brand HealthPresence Recalled by Cisco Systems Inc Due to Software...
The Issue: Software anomaly may result in incorrect values and interpretations. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visual-ICE¿ Cryoablation System Recalled by Galil Medical, Inc. Due to Galil...
The Issue: Galil Medical is recalling a number of Visual Ice Cryoablation Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE Monitor B850 Product Usage: The CARESCAPE TM Monitor B850 Recalled...
The Issue: GE Healthcare become aware of 4 potential issues associated with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cliniqa Liquid QCTM Cardiac Marker Control for i-STAT Level 1 Recalled by...
The Issue: Abbott Point of Care (APOC) has determined that for the Cliniqa Liquid QC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00-4309-028-01 - Trabecular Metal Reverse Shoulder Liner 40mm 65¿ Neck...
The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.