Stryker recalls AHTO Tube Set with Tip Packaging (Catalog 0250070620) due to reported leaks during use. Affected units include specific batch numbers. Consumers should check their product details.
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Stryker is recalling AHTO Tube Sets with Tip Packaging that have been reported to leak during use. This could cause contamination or damage to your dental equipment. If you own this product, stop using it and contact Stryker for a replacement.
The tube set leaks during use, which could lead to contamination of dental equipment or materials. This might cause infections or damage to the device, but the leaks are not reported to cause serious injury in normal use.
Dental professionals and their patients who use the recalled AHTO Tube Set with Tip Packaging are most at risk. The product is used in dental procedures, so anyone with this specific model should check if they have it.
Check for the catalog number 0250070620 on the product packaging. Affected units include specific batch numbers listed in the recall notice, such as 24263FG2 through 25157FG2.
Look for the catalog number 0250070620 and the batch numbers listed in the recall notice to confirm if your product is affected.
Reach out to Stryker Corporation for a replacement or repair if your product is confirmed to be affected by the recall.
The recall states there have been reported leaks during use, but it does not indicate that the leaks cause serious injury. Use caution if you have this product.
Affected batch numbers include 24263FG2 through 25157FG2 as listed in the recall notice.
Contact Stryker Corporation directly for a replacement if your product is confirmed to be affected by the recall.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2863-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2863-2026 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.
