Stryker recalls single spike tube sets with catalog number 0250070530 due to reported leaks during use. Affected units include specific batch numbers and GTIN.
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Stryker is recalling single spike tube sets that have been reported to leak during use. This could lead to potential contamination or damage if the leak occurs while in operation.
The product has been reported to leak during use, which could cause contamination or damage to the dental equipment. Leaks may occur when the tube set is in operation, potentially affecting the functionality of the dental handpiece.
Users of dental handpieces that use this specific tube set are affected. Dentists and dental technicians who have purchased the recalled product are most at risk.
Check for the catalog number 0250070530 on the product packaging. The affected units include specific batch numbers listed in the recall notice.
Look for the catalog number 0250070530 and the listed batch numbers on the product packaging.
Stryker has recalled the product due to reported leaks during use, which could lead to contamination or damage.
Check for the catalog number 0250070530 and the specific batch numbers listed in the recall notice.
The recall does not specify a remedy, so contact Stryker directly for further instructions.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2865-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2865-2026 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.
