Device recalls

Synchro .014"guide wire, 35 cm tip, Catalog: M00313010 Synchro .014 guide wire, 300 cm length, Catalog: M00313310 SYNCHRO .010 WIRE SOFT ST…

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-1909-2024
Open FDA's page for this record
Cfres ID
207253
Product res number
Z-1909-2024
Event date initiated
2024-04-23
Event date posted
2024-05-28
Recall status
Open, Classified
Res event number
94437
Product code
DQX
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
2859
Product description

Synchro .014"guide wire, 35 cm tip, Catalog: M00313010 Synchro .014 guide wire, 300 cm length, Catalog: M00313310 SYNCHRO .010 WIRE SOFT STRAIGHT 200cm, Catalog: M00316310 SYNCHRO .010 WIRE SOFT STRAIGHT 300cm, Catalog: M00316330

Code info

Catalog/UDI-DI/Lot: M00313010/07613252186922/123279, 123364, 123404, 123985, 124214, 124216; M00313310/07613252186946/123494; M00316310/07613252187158/123851; M00316330/07613252187165/124156

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
K023700, K002907
Harmonized identifiers (openFDA)
Device name
Wire, Guide, Catheter
Medical specialty description
Cardiovascular
Regulation number
870.1330
Device class
2
K number
K171997, K862360, K981381, K230418, K880287, K852123, K053187, K905581, K051062, K041762, K834237, K890404, K924558, K965140, K132623, K241510, K971688, K983506, K931171, K182985, K974560, K121745, K120863, K030019, K083727, K032050, K221351, K924385, K143135, K173052, K860533, K141295, K021243, K043398, K251596, K241702, K221917, K020821, K111395, K160018 +729 more
Registration number
3011469355, 3009092139, 1064858, 1649869, 2182208, 3003084417, 3009564766, 1313046, 9614758, 1030451, 3004111573, 3009756153, 2024168, 3010273872, 3014656749, 1721686, 3013750125, 3007830707, 3006425876, 3015531723, 3020954746, 2183744, 3011642792, 3035372913, 3004748528, 1319211, 2029214, 3007064586, 3018070217, 2134285, 3003289691, 3011564431, 3008264254, 3013943846, 1644312, 9612812, 3015225571, 3030452144, 3041276591, 8010026 +221 more
FEI number
3011469355, 3009092139, 3003084417, 2182208, 3009564766, 1313046, 1030451, 3004111573, 3009756153, 2024168, 3001451463, 3010273872, 3014656749, 1721686, 3013750125, 3007830707, 3006425876, 3015531723, 3001452571, 3020954746, 2183744, 3011642792, 3035372913, 3004748528, 1319211, 3007064586, 1000514656, 3018070217, 3003289691, 1000306431, 3008264254, 3011564431, 3013943846, 3015225571, 3030452144, 3004635528, 3041276591, 1028232, 1000563940, 1417485 +220 more
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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.