Lower risk Medical device recall · FDA · Published December 21, 2017

Stryker Disposable Cannula Recall: Expired Units Risk

Stryker recalls 5-unit boxes of disposable cannulas with expired expiration dates (August 2018 marked but should be 2016). Affected units may pose safety risks if used after expiration.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2057-2018Medical device Stryker ›

Lower-risk recall

Inadvertent shipment of expired units.

Take action

Contact the company

Recalling firmStryker Corporation5900 Optical Ct · San Jose, CA 95138-1400

✎ GovInfoNow plain-language explainer

Stryker is recalling 5-unit boxes of disposable cannulas that were shipped with expired expiration dates. Using expired medical devices could lead to safety issues if the product is no longer effective. Read more at govinfonow.com/recall/72242-stryker-disposable-cannula-recall-expired-units-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/72242-stryker-disposable-cannula-recall-expired-units-risk · Updated August 31, 2026 · FDA enforcement record: FDA #Z-2057-2018

Cite this page

“Stryker Disposable Cannula Recall: Expired Units Risk.” GovInfoNow, updated August 31, 2026. https://govinfonow.com/recall/72242-stryker-disposable-cannula-recall-expired-units-risk. Based on FDA recall #Z-2057-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2057-2018%22&limit=1).

The FDA announced on 2017-12-21 that Stryker Corporation is recalling Disposable Cannula devices due to the inadvertent shipment of expired units. The agency issued recall number Z-2057-2018 for the Class II device distributed in Massachusetts.

How to tell if you have it

Brand: Stryker
Product: 3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box
UPC: 07613327055795
Lot No.: 14239AG2
Distribution: US distribution to Massachusetts only

The hazard

The recall addresses the inadvertent shipment of expired units. The expiration date marked on the box is August 2018, but it should be August 2016.

Context

GovInfoNow's records show Stryker Corporation has 34 other recalls on record since 2017-11-17. Other recent recalls of similar products include Cook Medical Multipurpose Drainage Catheter Recall (2026-03-05), Cook Medical Wayne Pneumothorax Tray Recall (2026-03-05) and Cook Medical Spectrum Central Venous Tray Recall (2026-03-05).

How to tell if you have this one

Check for the model number 3910-090-800 on the box. The expiration date marked on the box is August 2018, but it should be August 2016. The product comes in boxes of 5 units.

Brand
Stryker
Product
3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Disposable Cannula device is
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Expiration Date
Verify the expiration date on the box is August 2016, not August 2018.

Where it went and when

Where it was distributed

Distributed in Massachusetts.

FDA distribution: “US distribution to Massachusetts only..” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Massachusetts.

Recall timeline

FDA published this recall 6 months after the firm started it.

Dec 21, 2017Firm started the recall
Jun 1, 2018FDA classified it Class II
Jun 13, 2018Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

Similar recalls

Latest medical device recalls

Keep exploring

More Stryker recalls

Link to this recall

<a href="https://govinfonow.com/recall/72242-stryker-disposable-cannula-recall-expired-units-risk">Stryker Disposable Cannula Recall: Expired Units Risk (GovInfoNow)</a>

Where this comes from

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-2057-2018 (December 21, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2057-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 31, 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.