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. 2,348 recalls have been distributed to Wyoming in the last 12 months.
Showing 33821–33840 of 48,219 recalls
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548850 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549390 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548560 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548750 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548920 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moog Curlin Infusion Recalled by MOOG Medical Devices Group Due to Moog is...
The Issue: Moog is recalling Curlin 4000, 6000, and PainSmart Infusion Pumps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: STD KIT GK260 Recalled by Applied Medical Resources Corp Due to Applied...
The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STD KIT GK213 Recalled by Applied Medical Resources Corp Due to Applied...
The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STD GK258 Recalled by Applied Medical Resources Corp Due to Applied Medical...
The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CA500 Epix Universal Clip Applier Product Usage: The Epix disposable...
The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Plaza Picture archiving and communication system. Software only. PACS...
The Issue: Siemens is releasing an updated software version to address several software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Symbiq infusion pump is a device used in a Recalled by Hospira Inc. Due...
The Issue: Potential for the Symbiq pole clamp assemblies to be missing the rubber stop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOLIS Microplate System Recalled by Bio-Rad Laboratories, Inc. Due to The...
The Issue: The error "Washer Reagent Clean Fluid" level low alarmed, which prompted the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number:...
The Issue: Drager became aware of situations where the error message "Poti unplugged"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.