Every recall we track for Stryker, Inc. — 2 in all — plus the complaints and injury reports the public filed about them.
Stryker recalls specific Trevo Pro 18 Microcatheters due to unapproved FDA use. Affected units have UDI and lot numbers listed. No remedy details provided in official notice.
Stryker recalls specific Trevo Trak 21 Microcatheter models due to unapproved FDA use. Affected units have unique lot numbers; contact Stryker for details.
