medical MODERATE Updated 2026-08-12

Stryker Corporation recalls STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0

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Recalled Product

STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0250070640

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Hazard / Issue

There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: GTIN 07613327061475, Batch Number: 24284FG2, 24289FG2, 24313FG2, 24322FG2, 24338FG2, 24344FG2, 24351FG2, 25009FG2, 25036FG2, 25062FG2, 25091FG2, 25129FG2, 25161FG2.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for STRYKER AHTO DUAL SPIKE →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

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