Medtronic Neurosurgery: Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2, 61100; DUREPAIR DURA SUBSTITUTE 3 X 3, 61105; DUREPAIR DURA SUBSTITUTE 1 X 3, 61106; DUREPAIR DURA SUBSTITUTE 4 X 5, 61110; DUREPAIR DURA SUBSTITUTE 1 X 1, 61111; DURA 62100 SUBSTITUTE DUREPAIR 2X2IN NCE, 62100; DURA 62105 SUBSTITUTE DUREPAIR 3X3IN NCE, 62105; DURA 62106 SUBSTITUTE DUREPAIR 1X3IN NCE, 62106; DURA 62110 SUBSTITUTE DUREPAIR 4X5IN NCE, 62110; DURA 62111 SUBSTITUTE DUREPAIR 1X1IN NCE, 62111; DURA 62158 SUBSTITUTE DUREPAIR 5X8IN NCE, 62158.

Recall number

Z-2207-2023

Recalling firm

Medtronic Neurosurgery

Product

Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2, 61100; DUREPAIR DURA SUBSTITUTE 3 X 3, 61105; DUREPAIR DURA SUBSTITUTE 1 X 3, 61106; DUREPAIR DURA SUBSTITUTE 4 X 5, 61110; DUREPAIR DURA SUBSTITUTE 1 X 1, 61111; DURA 62100 SUBSTITUTE DUREPAIR 2X2IN NCE, 62100; DURA 62105 SUBSTITUTE DUREPAIR 3X3IN NCE, 62105; DURA 62106 SUBSTITUTE DUREPAIR 1X3IN NCE, 62106; DURA 62110 SUBSTITUTE DUREPAIR 4X5IN NCE, 62110; DURA 62111 SUBSTITUTE DUREPAIR 1X1IN NCE, 62111; DURA 62158 SUBSTITUTE DUREPAIR 5X8IN NCE, 62158.

Status

Open, Classified

Initiated

2023-06-13

Posted

2023-07-20

Terminated

not on file

Reason

Dura regeneration matrix may have out-of-specification endotoxin levels due to issues with in-process and finished goods endotoxin testing, which may present clinically with signs and symptoms of an acute inflammatory process, comparable to infection.

Root cause

Process change control

Action

On 6/13/23 recall notices were mailed to customers and distributors and they were asked to do the following: 1) Return affected product to the recalling firm. 2) Complete and return the Customer Confirmation Form to neuro.quality@medtronic.com 3) This notice should be passed on to all those who need to be aware within your organization or to any organization where the potentially affected devices have been transferred. Please maintain a copy of this notice in your records. Customers with questions can contact Customer Service at 800-874-5797 Option 1.

Quantity

65029

Distribution

Worldwide - US Nationwide distribution including in the states of PR, TX, WA, HI, MI, GA, AL, IL, IN, IA, MO, KY, NY, CA, AZ, PA, UT, ME, MD, MN, FL, AK, NE, VA, OR, WI, NC, LA, SD, TN, MS, DE, NJ, ID, SC, OH, MA, DC, NM, WV, NH, CT, NV, OK, AR, KS, MT, RI, CO, ND, WY, VT and the countries of Barbados, Cayman Islands, Honduras, Belgium, Switzerland, Italy, United Kingdom, Canary Islands, Hungary, Poland, Germany, Spain, Czech Republic, Thailand, South Africa, Greece, Finland, Portugal, Colombia, Norway, Iraq, Jordan, Estonia, Austria, Slovakia, Libya, Qatar, Bosnia And Herzegovina, Algeria, Dominican Republic, Canada, Australia, New Zealand, Sweden, El Salvador, Ireland, United Arab Emirates, Saudi Arabia, Kazakhstan, Turkey, Mauritius, Ghana, Russian Federation, Lebanon, Romania, Iran, Islamic Republic Of, Egypt, Namibia, Senegal, Ecuador, Panama, Peru, Guyana, Mexico, Chile, Costa Rica, Viet Nam, Kuwait, Ukraine, Israel, Turkmenistan.

Lot, serial or model codes

REF/Expiration Date On or Prior/UDI-DI/Lots: 61100/March 31, 2025/00643169063808/2006039, 2007020, 2009028, 2010001, 2010016, 2102001, 2102020, 2103001, 2105028, 2106001, 2108011, 2108017, 2109022, 2110009, 2110030, 2111023, 2111045, 2112026, 2203020, 2204016, 2204035, 2207014, 2207046; 61105/February 28, 2025/00643169063815/2009060, 2011017, 2102011, 2102027, 2102047, 2103002, 2104042, 2105029, 2108001, 2108012, 2108016, 2109023, 2110010, 2111021, 2111024, 2111046, 2112027, 2202034, 2203034, 2204027, 2206008, 2207015, 2207033; 61106/December 31, 2024/00643169063822/2010017, 2103003, 2105030, 2105038, 2108013, 2108018, 2109004, 2110011, 2110031, 2111025, 2202035, 220302; 61110/March 31, 2025/00643169063839/2006039, 2010018, 2101014, 2102002, 2102028, 2103004, 2105031, 2108019, 2109024, 2110012, 2111026, 2201005, 2202036, 2204025, 2204040; 61111/April 30, 2025/00643169063846/2008039, 2010019, 2102021, 2103005, 2105032, 2106004, 2108014, 2110013, 2111027, 2202037, 2203022, 2203028, 2207016; 62100/January 31, 2025/00643169063853/2007021, 2008040, 2009026, 2009061, 2010014, 2011018, 2012001, 2101015, 2101020, 2102012, 2102022, 2102048, 2103019, 2104043, 2105033, 2106005, 2108020, 2109001, 2109020, 2109028, 2110014, 2110032, 2110033, 2111028, 2111035, 2111037, 2112001, 2112002, 2202038, 2203023, 2204001, 2204028, 2206013, 2206027, 2207017, 2207048, 2208009; 62105/January 31, 2025/00643169063860/2008005, 2008041, 2009029, 2010015, 2010020, 2012002, 2101016, 2102003, 2102013, 2102029, 2103006, 2103036, 2104044, 2105036, 2106035, 2108003, 2108015, 2109002, 2109003, 2110003, 2110015, 2110016, 2111022, 2111033, 2111047, 2201006, 2202014, 2202025, 2203015, 2203025, 2203031, 2204023, 2204036, 2204041, 2206014, 2206028, 2207018, 2207044; 62106/December 31, 2024/00643169063877/2008042, 2010021, 2101017, 2102023, 2103007, 2104045, 2105039, 2106007, 2108004, 2108021, 2109005, 2110017, 2110034, 2111029, 2202039, 2207019, 2207051; 62110/March 31, 2025/00643169063884/2006041, 2007022, 2008006, 2008043, 2010022, 2101009, 2101018, 2102026, 2102049, 2103020, 2104046, 2105001, 2105040, 2108005, 2108022, 2110004, 2110018, 2111036, 2201007, 2202015, 2202031, 2204017, 2204042, 2205031, 2205032, 2206007, 2207020, 2207049; 62111/May 31, 2025/00643169063891/2010023, 2012003, 2101019, 2102024, 2103008, 2105034, 2106009, 2108023, 2109006, 2110019, 2110035, 2111030, 2111034, 2202040, 2203024, 2204002, 2207021, 2207037, 2208027; 62158/April 30, 2025/00643169063907/2011019, 2103009, 2105035, 2110020, 2111031, 2202041, 2203033, 2204029, 2207006

510(k) numbers

["K161370"]

PMA numbers

not on file

Product code

GXQ

Firm FEI

3015531529

Firm city

Irvine

Firm state

CA

Firm country

not on file

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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