Lower riskMedical device recall · FDA · Published September 13, 2023
Stry: Portal Entry Kit with Expired Product Recalled
Stryker recalls Portal Entry Kit (lot #007047) due to expired product. This kit includes skin marker, ruler, FlexSticks, syringe and needles. No action needed as expired product is not a safety hazard.
“Stry: Portal Entry Kit with Expired Product Recalled.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/57325-stry-portal-entry-kit-with-expired-product-recalled. Based on FDA recall #Z-0287-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0287-2024%22&limit=1).
The FDA announced on 2023-09-13 that Stryker Corporation voluntarily recalled 19 Portal Entry Kits due to expired product distribution. GovInfoNow's records show this Class II recall involves kits distributed in New Hampshire, Texas, New York, New Jersey, Ohio, and Minnesota.
How to tell if you have it
Brand: Stryker
Product: Portal Entry Kit (REF: CAT00241)
Lot #: 007047
UDI: 07613252632863
The hazard
The recall involves expired product distribution, according to the FDA. The Portal Entry Kit consists of a skin marker, disposable ruler, (2) FlexSticks, 30 ml syringe, and (2) 17 Ga Needles used to aid surgeons in establishing arthroscopic portals.
Context
GovInfoNow's records show Stryker Corporation has 34 other recalls on record since 2017-11-17. Other recent recalls of similar products include Stryker Irrigator Leaks During Use (2026-06-08), Stryker Neptune Smart Docking Station Recall (2026-05-06), and Stryker FluidSmart Urology Tube Set Recall (2026-04-09).
How to tell if you have this one
This kit includes a skin marker, disposable ruler, two FlexSticks, 30 ml syringe, and two 17 Ga needles. Lot number 007047 (UDI: 07613252632863) is associated with this recall.
Brand
Stryker
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Lot Number
Look for lot number 007047 on the kit's packaging or label.
Where it went and when
Where it was distributed
Distributed in 6 states.
Listed by the agency
Not listed
FDA distribution: “US: NH, TX, NY, NJ, OH, MN OUS: None” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Minnesota, New Hampshire, New Jersey, New York, Ohio, Texas.
Recall timeline
FDA published this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-0287-2024 (September 13, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0287-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.