Device recalls

Trevo Pro 14 Microcatheter, Catalog: 90231; Trevo Pro 18 Microcatheter, Catalog: 90238

Stryker Neurovascular · Neurovascular devices did not meet the minimum sample size required for endotoxin testing during manufacturing processes and are out of compliance with the AAM…

Open, ClassifiedProcess designZ-1904-2024
Open FDA's page for this record
Cfres ID
207236
Product res number
Z-1904-2024
Event date initiated
2024-04-23
Event date posted
2024-05-28
Recall status
Open, Classified
Res event number
94437
Product code
DQO
Product description
Trevo Pro 14 Microcatheter, Catalog: 90231; Trevo Pro 18 Microcatheter, Catalog: 90238
Code info
Catalog/UDI-DI/Lot: 90231/00815742002317/121050, 129849, 129882, 130285, 136439, 136628, 143375, 143476; 90238/00815742002386/136009, 198334
Firm FEI number
3008853977
Recalling firm
Stryker Neurovascular
Address 1
47900 Bayside Pkwy
City
Fremont
State
CA
Postal code
94538-6515
Root cause description
Process design
Product quantity
648
Reason for recall

Neurovascular devices did not meet the minimum sample size required for endotoxin testing during manufacturing processes and are out of compliance with the AAMI ST72 standard, so these devices may exceed the acceptable limits of endotoxin levels; high levels of endotoxins may increase the risk of fever, shock and aseptic meningitis.

Action

On 4/23/24, recall notices were mailed to Supply Chain Management, Recall Coordinators, and Inventory Managers who were asked to do the following: 1) Cease further distribution or use of all affected devices. 2) Segregate the affected units in a secure location for return to the firm. 3) Circulate this Recall-Removal notice internally to all interested/affected parties. 4) Maintain awareness of this communication internally until all required actions have been completed within your facility. 5) Inform the firm if any of the subject devices have been distributed to other organizations. If yes, provide contact details so the firm can inform the recipients appropriately. 6) Inform the firm of any adverse events concerning the use of the subject devices. (US Customer Service: 1-855-91-NEURO (1-855-916-3876), Email: NVCustomerCare@stryker.com) 7) Complete and return the response form via email to nvfieldactions@stryker.com

Distribution pattern

Worldwide - US Nationwide distribution including in the states of MN, PA, IL, AK, NY, CA, MI, WI, TX, AZ, FL, KY, MA, IN, NE, MT, CT, NJ, TN, VA, AL, CO, DE, OH, UT, NC, ME, GA, SC, GU, WA, MO, OR, DC, OK, LA, MD, ID, NH, SD, NV, RI, ND, HI, MS, AR, IA, NM, VT, KS and the countries of Australia, Austria, Belgium, Brazil, Canada, Canary Islands, Chile, China, Czech Republic, Denmark, Finland, France, Germany, Hong Kong, SAR China, Hungary, India, Ireland, Israel, Italy, Japan, Korea (South), Lithuania, Luxembourg, Netherlands, Northern Ireland, Norway, Poland, Portugal, Romania, Russian Federation, Saudi Arabia, Singapore, Slovakia, Spain, Sweden, Switzerland, Taiwan, Republic of China, Thailand, Turkey, United Arab Emirates, United Kingdom.

K numbers
K131437, K113260
Harmonized identifiers (openFDA)
Device name
Catheter, Intravascular, Diagnostic
Medical specialty description
Cardiovascular
Regulation number
870.1200
Device class
2
K number
K944284, K914009, K885348, K974559, K790107, K052637, K911703, K823758, K060116, K860429, K801321, K230620, K930479, K212977, K993694, K041291, K062627, K911270, K150232, K771810, K813623, K830523, K133130, K942939, K171264, K981441, K024126, K770290, K121694, K193647, K830788, K853182, K173762, K012983, K915726, K854018, K131770, K841615, K041909, K884354 +461 more
Registration number
8020616, 3003678543, 3013351723, 3004111573, 2024168, 1646831, 3014656749, 1721686, 3007830707, 3006425876, 3014779787, 2183744, 3011642792, 1319211, 2029214, 3008264254, 3006950086, 3015225571, 3004122598, 8010026, 9616683, 3012494290, 1928237, 1055236, 3005669815, 2521402, 9616099, 3008496528, 3011660785, 3004605321, 1058584, 3012497308, 1061927, 9612152, 2528981, 3007289408, 3005941719, 3021343210, 1123137, 9618000 +171 more
FEI number
3003678543, 3013351723, 3002806476, 3004111573, 2024168, 3014656749, 1721686, 3004970277, 3007830707, 3006425876, 3014779787, 2183744, 3011642792, 1319211, 1000514656, 3003807466, 1000306431, 3008264254, 3006950086, 3015225571, 3004122598, 3003040625, 3012494290, 1928237, 1000112877, 3005669815, 3016261803, 2521402, 3004605321, 3008496528, 3011660785, 3002534070, 3003094851, 3012497308, 1000512168, 3007289408, 2528981, 3002807548, 3021343210, 3004467263 +170 more
Wholesale access for licensed clinicians.

Free to join: your NPI is checked against the federal registry at signup, then wholesale pricing and the professional shelves open.

Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.