Devices

Device Recall KODAK DirectView DR 7500 Dual Detector System, MODEL DR 7500

Model / Serial
Service Code: 8087; Catalog numbers: 8791345, 1155118, 1295088, 8551046, 8791345, 1666700, 8531675
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
worldwide Distribution - US (Nationwide) including states of: IN, PA, MD, MI, NY, GA, MN, OK, VA, TX, WI, CA, IL, TN, WA, NC, SC, MA, NJ, and KY; and Internationally to: Canada, New Zealand, South Korea, Australia, Hong Kong, Saudia Arabia, Guinea, Kuwait, Israel, Oman, South Africa, China, UK, Sweden, Poland, Denmark, Germany, Finland, Czech Republic, Italy, France, Portugal and Spain.
Product Description
KODAK DirectView DR 7500 Dual Detector System, MODEL DR 7500, Manufactured by Carestream Health, Inc. Made in U.S.A.
Manufacturer
Carestream Health, Inc.
1 Event
- Recall of Device Recall KODAK DirectView DR 7500 Dual Detector System, MODEL DR 7500

Manufacturer

Carestream Health, Inc.

Manufacturer Address
Carestream Health, Inc., 1049 Ridge Rd W, Rochester NY 14615-2731
Manufacturer Parent Company (2017)
ONEX Corp
Source
USFDA

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