Dukal Corp. Recalls Sterile Burn Sheets Due to Shredded Sheets
Dukal Corp. recalls sterile burn sheets (Item 7305) with shredded sheets in carton. Affected lots include JT13607 to JT36212. Consumers should check lot numbers and contact for details.
Lower-risk recall
Intact carton revealed presence of shredded burn sheets
Contact the company
What happened, in plain English
Dukal Corp. is recalling sterile burn sheets that may have shredded sheets inside the carton. This could lead to contamination or infection risks for patients during medical procedures. Read more at govinfonow.com/recall/73981-dukal-corp-recalls-sterile-burn-sheets-due-to-shredded-sheets.
Source Summary by GovInfoNow · govinfonow.com/recall/73981-dukal-corp-recalls-sterile-burn-sheets-due-to-shredded-sheets · Updated September 23, 2026 · FDA enforcement record: FDA #Z-0233-2018
Cite this page
“Dukal Corp. Recalls Sterile Burn Sheets Due to Shredded Sheets.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/73981-dukal-corp-recalls-sterile-burn-sheets-due-to-shredded-sheets. Based on FDA recall #Z-0233-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0233-2018%22&limit=1).
Why it’s dangerous
The burn sheets may have shredded pieces inside the carton, which could contaminate the sterile product. This poses a risk of infection if the sheets are used without proper cleaning or handling.
Who’s affected
Patients using sterile burn sheets for medical procedures are most at risk. Healthcare providers who use these sheets in patient care may also be affected.
How to tell if you have this one
Check the carton for shredded sheets. The product is labeled as 'BLUE BURN SHEET, STERILE, 60" x 96"; Item 7305, GAM item 30-01'. Affected lots include specific numbers starting with JT followed by 8 digits.
- Brand
Dukal Corp.- Category
Medical device
What to do — step by step
Check Carton for Shredded Sheets
Inspect the carton for shredded sheets before use. If present, do not use the product.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 15 states.
FDA distribution: “Worldwide distribution - US Nationwide in the states of: CA, CO, CT, FL, GA, IL, CO, NY, NV, IN, MD, MO, MD OH, TN, TX & WI; and country of Canada” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Colorado, Connecticut, Florida, Georgia, Illinois, Indiana, Maryland, Missouri, Nevada, New York, Ohio, Tennessee, Texas, Wisconsin.
Recall timeline
FDA terminated this recall 14 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
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-0233-2018 (June 1, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0233-2018 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 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.