FDA Recall Terminated

Medtronic SynchroMed EL Programmable Pump, Model 8627-18. Medtronic, Inc., 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA.--(The implantable Medtronic SynchroMed EL Programmable Pump is part of the SynchroMed EL Infusion System designed to contain and administer parenteral drugs to a specific site)

Recall: Z-0745-2008 · Initiated August 3, 2007

Recall

Recall Number
Z-0745-2008
Event Number
36595
Firm
Medtronic Neuromodulation
FEI Number
2182207
Product Code
LKK
Status
Terminated
Root Cause
Device Design
Initiated
August 3, 2007
Posted
February 2, 2008
Terminated
June 6, 2011
Address
800 53rd Ave NE PO Box 1250, Minneapolis, MN, 55440-1250

Description

Medtronic SynchroMed EL Programmable Pump, Model 8627-18. Medtronic, Inc., 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA.--(The implantable Medtronic SynchroMed EL Programmable Pump is part of the SynchroMed EL Infusion System designed to contain and administer parenteral drugs to a specific site)

Reason

Pump motor stall due to gear shaft wear

Action

Beginning August 3, 2007, consignees were notified by letter. The letter "Medtronic Urgent: Medical Device Correction Aug 2007" described the problem and the Affected Devices as well as Patient Risk, Patient Management Recommendations, Next Steps and Physician and Patient Support.

Distribution

Worldwide: USA including states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY and countries of HONG KONG, AUSTRALIA, CANADA, AUSTRIA, BELGIUM, CROATIA, The CZECH REPUBLIC, DENMARK, EGYPT, FINLAND, FRANCE, GERMANY, HUNGARY, IRAN, ICELAND, IRELAND, ITALY, THE NETHERLANDS, NORWAY, POTUGAL, SAN MARINO, SAUDI ARABIA, SPAIN, SWEDEN, SWITERLAND, TURKEY, UNITED ARAB EMIRATES, UNITED KINGDOM, IRAQ, BRAZIL, and MEXICO.

Quantity

23, 895 total for recalls Z-0739-0746-2008