Stryker recalls Ahto Dual Spike Tube Set packaging (Catalog 0250070640) due to reported leaks during use. Affected units include specific batch numbers. Contact Stryker for details.
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Stryker is recalling Ahto Dual Spike Tube Set packaging because it has been reported to leak during use. This could lead to potential contamination or damage to the device if not addressed.
The packaging has been reported to leak during use, which could lead to contamination or damage to the device. Leaks may cause the product to become ineffective or pose a risk of cross-contamination.
Users of the Ahto Dual Spike Tube Set packaging with the specified catalog number and batch numbers are affected. Dental professionals using this product are most at risk.
Check for the catalog number 0250070640 on the packaging. Affected units include batch numbers 24284FG2 through 25161FG2.
Look for the catalog number 0250070640 and batch numbers 24284FG2 through 25161FG2 on the packaging.
Stryker has reported an increased number of complaints about leaks from the handpiece during use.
Check the packaging for the catalog number 0250070640 and batch numbers 24284FG2 through 25161FG2. Contact Stryker for further instructions.
The recall record does not mention a remedy or fix.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2864-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2864-2026 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
