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. 1,997 recalls have been distributed to Wyoming in the last 12 months.
Showing 4241–4260 of 27,462 recalls
Recalled Item: RayStation 14.0.0.3338. Radiation Therapy Treatment Planning System....
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain Recalled by...
The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain Recalled by...
The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Universal Connector PVC Tubing Anti Transparent Y Recalled by...
The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newport s N-LHP-928(j) units if sold as a laser head/power supply set...
The Issue: According to 21 CFR 1040.10(f)(4), each laser system classified as a Class...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain Recalled by...
The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt 3-Spring Reservoir with Silicone Adapters Recalled by Cardinal...
The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stealth S8 Clinical Software Application Recalled by Medtronic Navigation,...
The Issue: Due to a software issue, there is the potential for a missing digit, letter,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP V30 Auto Ventilator Recalled by Philips Respironics, Inc. Due to...
The Issue: Potential for devices to experience interruption/loss of therapy during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP A30 Ventilator Recalled by Philips Respironics, Inc. Due to Potential...
The Issue: Potential for devices to experience interruption/loss of therapy during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP A40 Ventilators: BiPAP A40 Recalled by Philips Respironics, Inc. Due...
The Issue: Potential for devices to experience interruption/loss of therapy during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RKN130003 Recalled by Ossur H / F Due to Due to firmware issues with the...
The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RKN130002 Recalled by Ossur H / F Due to Due to firmware issues with the...
The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RKNXC0005 Recalled by Ossur H / F Due to Due to firmware issues with the...
The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RKNXC0003 Recalled by Ossur H / F Due to Due to firmware issues with the...
The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5000 Compact Series Ultrasound Systems Recalled by Philips Ultrasound, Inc....
The Issue: Ultrasound system with: 1) transesophageal echocardiography transducer (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the...
The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20" Lead Wires Recalled by EBI, LLC Due to Damage to the lead wire sheath...
The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) ENDO KIT Recalled by...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) ANESTHESIA CIRCUIT...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.