Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Stryker CorporationLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Stryker Medical with 80 device recalls and 14 510(k) clearances. The most recent is a device recall dated Feb 18, 2026: Cub Pediatric Crib, Model FL19H.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Feb 18, 2026 | Cub Pediatric Crib, Model FL19HClass II · Cribs sold in the USA are missing two access door warning labels. | Device recalls |
| Oct 31, 2025 | Stryker Arise 1000EX mattress, Part Number 2236000000Class II · Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products hav | Device recalls |
| Oct 31, 2025 | Stryker MV3 bariatric bed, Part Number 5900000001Class II · Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products hav | Device recalls |
| Aug 30, 2023 | ProCuity bed series, model number 3009, item number: 3009PX-LE-400.Class II · Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock. | Device recalls |
| Aug 30, 2023 | ProCuity bed series, model number 3009, item number: 3009PX-L-100.Class II · Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock. | Device recalls |
| Aug 30, 2023 | ProCuity bed series, model number 3009, item number: 3009PX-ZM-450.Class II · Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock. | Device recalls |
| Aug 30, 2023 | ProCurity bed series, model number 3009, item number: 3009PX-ZMX-600.Class II · Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock. | Device recalls |
| Aug 30, 2023 | ProCuity bed series, model number 3009, item number: 3009PX-LEX-400.Class II · Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock. | Device recalls |
| Jan 24, 2023 | Xpedition ™ Powered Stair Chair (625700000000)K222818 · ILK | 510(k) clearances |
| Aug 10, 2018 | Altrix Precision Temperature Management SystemK180834 · DWJ | 510(k) clearances |
| Jul 18, 2017 | Altrix Temperature Management WrapsK171149 · DWJ | 510(k) clearances |
| Dec 2, 2016 | Altrix Precision Temperature Management SystemK152266 · DWJ | 510(k) clearances |
| Dec 20, 2011 | POWER-LOAD COT FASTENER SYSTEMK113598 · FPO | 510(k) clearances |
| Mar 14, 1995 | STRYKER AGILITY INTENSIVE CARE BEDK946149 · FNL | 510(k) clearances |
| Aug 25, 1994 | STRYKER 8000 SURGERY STRETCHERK943864 · FPO | 510(k) clearances |
| Jun 17, 1994 | STRYKER 5000K935949 · FNM | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
