Stryker Corporation: Apparatus, Suction, Operating-room, Wall Vacuum Powered
Recall Summary Stryker Corporation is recalling its AHTO Dual Spike Tube Set (catalog number 0250070640), a wall-mounted surgical suction apparatus used in operating rooms. The product is being recalled because multiple users have reported leaking from the handpiece during use. The recall affects units distributed worldwide, including throughout the United States and 18 other countries.
- Recalling firm
- Stryker Corporation
- Product
- STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0250070640
- Reason
- There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-06-08
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Worldwide distribution - US Nationwide and the countries of Australia, Brazil, Canada, Chile, France, Germany, Indonesia, Italy, Mexico, Netherlands, New Zealand, Philippines, South Korea, Spain, Sweden, Switzerland, Taiwan, United Kingdom.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/2e6dbf28-a619-4732-beff-dfed08223f4c