Mentor Syringe Luer Lok 10cc-200 Box Recall: Expired Syringes
Mentor recalls expired syringes due to distribution error. Affected items have specific product codes and lot numbers. Consumers should check their syringes for the lot number 8298877.
Lower-risk recall
A single lot of expired syringes were distributed due to a distribution system control failure.
Contact the company
What happened, in plain English
Mentor is recalling a specific batch of syringes that were distributed due to an expired lot number. This recall is important because using expired syringes could lead to contamination or infection risks. Read more at govinfonow.com/recall/49329-mentor-syringe-luer-lok-10cc-200-box-recall-expired-syringes.
Source Summary by GovInfoNow · govinfonow.com/recall/49329-mentor-syringe-luer-lok-10cc-200-box-recall-expired-syringes · Updated August 17, 2026 · FDA enforcement record: FDA #Z-2614-2026
Cite this page
“Mentor Syringe Luer Lok 10cc-200 Box Recall: Expired Syringes.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/49329-mentor-syringe-luer-lok-10cc-200-box-recall-expired-syringes. Based on FDA recall #Z-2614-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2614-2026%22&limit=1).
Why it’s dangerous
The syringes were distributed from a single expired lot due to a distribution system control failure. Using expired syringes can lead to contamination or infection risks, especially in medical settings.
Who’s affected
People who own or use the Mentor Syringe Luer Lok 10cc-200/Box with product code 302995 and lot number 8298877 are affected. Healthcare workers and medical professionals using these syringes are most at risk.
How to tell if you have this one
Check for the product code 302995 and lot number 8298877 on the syringe box. The syringe is labeled as 'Syringe, Piston' with Mentor Product Code B9604.
- Brand
Mentor- Product
SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 Syringe, Piston- Category
Medical device
What to do — step by step
Check Syringe Lot Number
Look for the lot number 8298877 on the syringe box or label.
Where it went and when
Where it was distributed
Distributed in 3 states.
FDA distribution: “U.S.: CA, FL, and PA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Florida, Pennsylvania.
Recall timeline
FDA published this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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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-2614-2026 (April 28, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2614-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 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.