Stryker recalls AHTO Tube Set Packaging (Catalog 0250070600) due to reported leaking from handpieces during use. Affected units include specific batch numbers.
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Stryker is recalling AHTO Tube Set Packaging with catalog number 0250070600 because it has been reported to leak during use. This could lead to potential contamination or damage to the device.
The packaging has been reported to leak during use, which could cause contamination or damage to the handpiece. This may lead to compromised dental procedures or device functionality.
Users of the Stryker AHTO Tube Set Packaging with specific batch numbers are affected. Dental professionals using these products are most at risk due to potential leaks during procedures.
Check for the catalog number 0250070600 on the packaging. Affected units include specific batch numbers listed in the recall notice.
Look for the catalog number 0250070600 and specific batch numbers listed in the recall notice.
Stryker has reported increased complaints of leaking from the handpiece during use.
Affected batch numbers include 24262FG2 through 25163FG2 as listed in the recall notice.
No specific action is required beyond checking the packaging details; the recall does not mandate immediate discontinuation.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2862-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2862-2026 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.
