Fresh Recalls

FDAClass II · Medical device · Recall Z-2863-2026 · Recalled August 12, 2026

STRYKER AHTO TUBE SET WITH TIP PACKAGING recall — Stryker Corporation

Agency report date: August 12, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
STRYKER AHTO TUBE SET WITH TIP PACKAGING
Company / brand
Stryker
Lot / serial / date codes
GTIN 07613327061659, Batch Numbers: 24263FG2, 24264FG2, 24265FG2, 24267FG2, 24269FG2, 24270FG2, 24271FG2, 24288FG2, 24289FG2, 24290FG2, 24291FG2, 24292FG2, 24296FG2, 24297FG2, 24298FG2, 24304FG2, 24306FG2, 24313FG2, 24317FG2, 24318FG2, 24319FG2, 24320FG2, 24327FG2, 24340FG2, 24341FG2, 24342FG2, 24343FG2, 24344FG2, 24345FG2, 24347FG2, 24348FG2, 24356FG2, 24357FG2, 24358FG2, 24361FG2, 25007FG2, 25010FG2, 25011FG2, 25015FG2, 25016FG2, 25017FG2, 25020FG2, 25021FG2, 25022FG2, 25023FG2, 25024FG2, 25027FG2, 25028FG2, 25030FG2, 25037FG2, 25038FG2, 25041FG2, 25042FG2, 25043FG2, 25049FG2, 25050FG2, 25051FG2, 25055FG2, 25065FG2, 25066FG2, 25069FG2, 25070FG2, 25071FG2, 25072FG2, 25073FG2, 25076FG2, 25077FG2, 25078FG2, 25079FG2, 25080FG2, 25083FG2, 25084FG2, 25085FG2, 25086FG2, 25090FG2, 25091FG2, 25092FG2, 25093FG2, 25097FG2, 25098FG2, 25098GF2, 25099FG2, 25100FG2, 25104FG2, 25105FG2, 25106FG2, 25111FG2, 25112FG2, 25127FG2, 25128FG2, 25129FG2, 25132FG2, 25133FG2, 25134FG2, 25139FG2, 25140FG2, 25141FG2, 25142FG2, 25143FG2, 25147FG2, 25148FG2, 25149FG2, 25150FG2, 25151FG2, 25153FG2, 25154FG2, 25155FG2, 25156FG2, 25157FG2.
Distribution
Worldwide distribution - US Nationwide and the countries of Australia, Brazil, Canada, Chile, France, Germany, Indonesia, Italy, Mexico, Netherlands, New Zealand, Philippines, South Korea, Spain, Sweden, Switzerland, Taiwan, United Kingdom.
Agency product description and boundaries

STRYKER AHTO TUBE SET WITH TIP PACKAGING, Catalog Number 0250070620

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: STRYKER AHTO TUBE SET WITH TIP PACKAGING

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID
Z-2863-2026
Brand
Stryker
Classification
Class II
Units affected
41,052 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
San Jose, CA, United States
Firm address
5900 Optical Ct, 95138-1400

Identifying details (verbatim from the notice)

Product codes / lots
GTIN 07613327061659, Batch Numbers: 24263FG2, 24264FG2, 24265FG2, 24267FG2, 24269FG2, 24270FG2, 24271FG2, 24288FG2, 24289FG2, 24290FG2, 24291FG2, 24292FG2, 24296FG2, 24297FG2, 24298FG2, 24304FG2, 24306FG2, 24313FG2, 24317FG2, 24318FG2, 24319FG2, 24320FG2, 24327FG2, 24340FG2, 24341FG2, 24342FG2, 24343FG2, 24344FG2, 24345FG2, 24347FG2, 24348FG2, 24356FG2, 24357FG2, 24358FG2, 24361FG2, 25007FG2, 25010FG2, 25011FG2, 25015FG2, 25016FG2, 25017FG2, 25020FG2, 25021FG2, 25022FG2, 25023FG2, 25024FG2, 25027FG2, 25028FG2, 25030FG2, 25037FG2, 25038FG2, 25041FG2, 25042FG2, 25043FG2, 25049FG2, 25050FG2, 25051FG2, 25055FG2, 25065FG2, 25066FG2, 25069FG2, 25070FG2, 25071FG2, 25072FG2, 25073FG2, 25076FG2, 25077FG2, 25078FG2, 25079FG2, 25080FG2, 25083FG2, 25084FG2, 25085FG2, 25086FG2, 25090FG2, 25091FG2, 25092FG2, 25093FG2, 25097FG2, 25098FG2, 25098GF2, 25099FG2, 25100FG2, 25104FG2, 25105FG2, 25106FG2, 25111FG2, 25112FG2, 25127FG2, 25128FG2, 25129FG2, 25132FG2, 25133FG2, 25134FG2, 25139FG2, 25140FG2, 25141FG2, 25142FG2, 25143FG2, 25147FG2, 25148FG2, 25149FG2, 25150FG2, 25151FG2, 25153FG2, 25154FG2, 25155FG2, 25156FG2, 25157FG2.
Distribution
Worldwide distribution - US Nationwide and the countries of Australia, Brazil, Canada, Chile, France, Germany, Indonesia, Italy, Mexico, Netherlands, New Zealand, Philippines, South Korea, Spain, Sweden, Switzerland, Taiwan, United Kingdom.
Firm notified the public via
Letter
FDA event ID
99340
Recall initiated
June 8, 2026
FDA classified
August 3, 2026
FDA report date
August 12, 2026
Verify with the official sources:

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

Report a data error on this page