Certified Safety Burn Sheets Recall: Risk of Shredding
Certified Safety recalls sterile burn sheets (60" x 96") that may shred, causing injury. Affected items include specific first aid kits. Stop using immediately.
Stop using this now
Burn Sheet has possibility of being shredded.
Contact the company
What happened, in plain English
Certified Safety is recalling sterile burn sheets that could shred, potentially causing injury. This affects first aid kits sold with specific model numbers. The recall is for safety reasons to prevent harm. Read more at govinfonow.com/recall/73564-certified-safety-burn-sheets-recall-risk-of-shredding.
Source Summary by GovInfoNow · govinfonow.com/recall/73564-certified-safety-burn-sheets-recall-risk-of-shredding · Updated September 21, 2026 · FDA enforcement record: FDA #Z-3078-2017
Cite this page
“Certified Safety Burn Sheets Recall: Risk of Shredding.” GovInfoNow, updated September 21, 2026. https://govinfonow.com/recall/73564-certified-safety-burn-sheets-recall-risk-of-shredding. Based on FDA recall #Z-3078-2017 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3078-2017%22&limit=1).
Why it’s dangerous
Burn sheets may shred during use, creating small pieces that could cause injury. This is a risk in medical settings where sterile environments are critical for patient safety.
Who’s affected
People using sterile burn sheets or first aid kits with the specified model numbers are affected. Medical professionals and patients using these products are at highest risk.
How to tell if you have this one
Check for the product name 'Burn Sheet' (60" x 96"), model numbers Dukal 7305 or CSM R505-091, or first aid kits with CSM part number K608-0:61. The sheets have a Certified Safety logo and were sold with specific lot numbers.
- Brand
Certified Safety- Category
Medical device
What to do — step by step
Stop Using Immediately
Discard any burn sheets or first aid kits with the specified model numbers and lot numbers to prevent injury.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 5 states.
FDA distribution: “US Nationwide Distribution in the states of KY, MD, NY, PA, VA” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Kentucky, Maryland, New York, Pennsylvania, Virginia.
Recall timeline
FDA terminated this recall 3.4 years 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-3078-2017 (June 26, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3078-2017 to see it in context.
- Plain-language summary written by qwen3:4b on September 21, 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.