Moog Medical Device Recall

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Medical Device Recalls | FDA

https://www.fda.gov/medical-devices/medical-device-safety/medical-device-recalls

Summaries of information about the most serious medical device recalls. These products are on the list because there is a reasonable chance that they could cause serious health problems or death.

Class 2 Device Recall Curlin Ambulatory Volumetric …

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=142508

Moog Medical Device Group sent an "Urgent Recall Notice" dated December 22, 2015, to all affected customers. The notice identified the product, the …

2022 Medical Device Recalls | FDA

https://www.fda.gov/medical-devices/medical-device-recalls/2022-medical-device-recalls

11/01/22. Philips Respironics Recalls Certain Masks for BiPAP, CPAP Machines Due to Safety Issue with Magnets That May Affect Certain Medical Devices. 10/18/22. Jiangsu …

MOOG MEDICAL DEVICES GROUP ANNOUNCES …

https://www.moog.com/content/dam/moog/literature/Medical/Administration_Set_Recall_5.22.12.pdf

MOOG INC., EAST AURORA, NEW YORK 14052 TEL-716/652-2000 FAX -716/687-4457 release date Immediate contact Ann Marie Luhr May 22, 2012 716-687- …

CURLIN Infusion and Infinity Enteral Feeding Pumps

https://www.moogmedical.com/

From 24 hour per day clinical support, to live stream training, self-paced e-Learning, and onsite education in your facility; our clinical and customer support teams offer the most …

Medical Device Recalls - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?start_search=1&knumber=K981816

Zevex Incorporated (dba MOOG Medical Devices Group) MOOG Curlin Infusion Administration Set, REF 340-4130-V, Non-DEHP Tubing with Non-Vented Bag Spike a...

Moog Recalls Curlin Ambulatory Infusion Pump Models …

https://www.moog.com/news/corporate-press-releases/2011/moog-recalls-curlin-ambulatory-infusion-pump-models-6000-cms-6000-cms-iod-painsmart-painsmart-iod.html

8 April 2011 East Aurora, NY– Moog Inc. (NYSE: MOG.A and MOG.B) announced today that the Food and Drug Administration (FDA) has classified the …

Support and Contact Information - Moog Medical

https://www.moogmedical.com/contact/

Moog Medical – USA 4314 Zevex Park Lane Salt Lake City, Utah 84123 USA tel: 801.264.1001 fax: 801.264.1051. Infusion Therapy CURLIN 6000 Pump CURLIN …

Medical OEM - Moog Inc.

https://www.moog.com/markets/medical-oem.html

The medical market is a market in motion – both literally and figuratively. With the Baby Boomers reaching retirement age and technology advancing almost exponentially, this is an …

GE HealthCare Recalls Nuclear Medicine 600/800 …

https://www.fda.gov/medical-devices/medical-device-recalls/ge-healthcare-recalls-nuclear-medicine-600800-series-systems-risk-detector-fall-may-injure-patients

See Medical Device Recall Database entry for more information. Distribution Dates: April 1, 2018 to December 16, 2022; Devices Recalled in the U.S.: 688; Date …

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