STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING recall (Stryker Corporation)
Medical deviceClass IIOngoing
Summary: Stryker Corporation is recalling 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.
What is being recalled
STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0250070640
Why
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
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.
How to tell if yours is affected
GTIN 07613327061475, Batch Number: 24284FG2, 24289FG2, 24313FG2, 24322FG2, 24338FG2, 24344FG2, 24351FG2, 25009FG2, 25036FG2, 25062FG2, 25091FG2, 25129FG2, 25161FG2.
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-2864-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | June 8, 2026 |
| Reported | August 12, 2026 |
| Company | Stryker Corporation |
| Company location | San Jose, CA, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 2,739 of units |
More recalls from Stryker Corporation · all medical device recalls · recalls from June 2026