Reported Feb 5, 2014 · Terminated
KODAK DirectView DR 7500 Dual Detector System, MODEL DR 7500, Manufactured by Carestream Health, Inc. Made in U.S.A.
Carestream Health, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Carestream Health, Inc. · 1049 Ridge Rd W · Rochester, NY · 14615-2731
Is this the product you have?
- KODAK DirectView DR 7500 Dual Detector System, MODEL DR 7500, Manufactured by Carestream Health, Inc. Made in U.S.A.
- Lot codes and dates
- Service Code8087
- Catalog numbers
8791345115511812950888551046879134516667008531675
- Amount recalled
- 164 units Total (42 domestically & 122 internationally)
Where it was sold
Why it was recalled
Carestream Health, Inc. has recalled DR 7500 Dual Detector System utilizing Version 5.X Software due to a possible patient image display error.
This product could cause temporary or reversible health problems — stop using it.
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