Stryker Corporation: Apparatus, Suction, Operating-room, Wall Vacuum Powered
Recall Summary Stryker Corporation is recalling its AHTO Tube Set (Catalog Number 0250070600), a wall-mounted operating room suction apparatus, due to reports of leaking from the handpiece during use. The product was distributed worldwide, including throughout the United States and 18 other countries. This is a Class II recall, meaning the product could cause serious adverse health consequences or death.
- Recalling firm
- Stryker Corporation
- Product
- STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600
- 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/f933e448-0b9e-45da-a3c4-6a6d6be899f2