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FDA Medical Device Recalls (openFDA)

Gambro Renal Products, Inc.: Gambro Prisma M100 preset, Part No. 8353486.

Recall number
Z-0705-06
Recalling firm
Gambro Renal Products, Inc.
Product
Gambro Prisma M100 preset, Part No. 8353486.
Status
Terminated
Initiated
2005-10-24
Posted
2006-04-05
Terminated
2012-04-17
Reason
After dialysis machine is disconnected from the patient, blood leakage may occur while unloading the tubing sets from the machine.
Root cause
Other
Action
Recall information was forwarded to all Gambro Sale Organizations. Notification was sent to all US consignees on November 2nd and November 3rd, 2005.
Quantity
28277 units
Distribution
Nationwide, including VA facilities in AZ, CA, DC, FL, GA, MI, MO, NJ, NY, OH, OR, PA, PR, TX, UT, VA, WI. Military distribution to CA and TX. Foreign distribution to Australia, Canada, Denmark, France, Germany, Hungary, UK.
Lot, serial or model codes
Lot numbers 04K2692P, 05A0754P, 05D1571, 05F0763A, 05F0865, 05F0966, 05F1573G, 05F1574, 05F1675G, 05F2387G, 05F3098G, 05G0556G, 05G0760G, 05G1366G. Recall expanded on 04/13/2006 to include 05AXXXXX through 05J2796P.
510(k) numbers
["K032431","K980386","K981681"]
PMA numbers
not on file
Product code
KDI
Firm FEI
1713683
Firm city
Lakewood
Firm state
CO
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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