Cenorin ThermaSure Series 300 Dryer: Overheating Risk
Cenorin recalls ThermaSure Series 300 medical device dryers (Models 330/340) with serial numbers listed due to overheating risk from terminal block failure.
Use caution until it’s fixed
Dryer unit not heating. Manufacturing issue causes the terminal block to overheat, char and/or burn.
Contact the company
What happened, in plain English
Cenorin is recalling two models of medical device dryers (330 and 340) because they can overheat and cause burns. This affects specific serial numbers listed in the recall notice. Read more at govinfonow.com/recall/73906-cenorin-thermasure-series-300-dryer-overheating-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/73906-cenorin-thermasure-series-300-dryer-overheating-risk · Updated September 23, 2026 · FDA enforcement record: FDA #Z-3033-2017
Cite this page
“Cenorin ThermaSure Series 300 Dryer: Overheating Risk.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/73906-cenorin-thermasure-series-300-dryer-overheating-risk. Based on FDA recall #Z-3033-2017 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3033-2017%22&limit=1).
Why it’s dangerous
The dryer's terminal block overheats due to a manufacturing defect, which can cause it to char and burn. This poses a fire or burn hazard during normal use.
Who’s affected
Medical facilities using ThermaSure Series 300 dryers with the listed serial numbers are most at risk. Owners of these specific models should check their serial numbers.
How to tell if you have this one
Check if your ThermaSure Series 300 dryer has a serial number from the list provided in the recall notice. The affected models are 330 and 340 with specific serial numbers listed.
- Brand
Cenorin- Category
Medical device
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Worldwide Distribution - US (Nationwide) Internationally to Japan, Hong Kong, Brunei, and Israel
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-3032-2017 | ThermaSure(TM), a CENORIN(TM) product, SERIES 130 MEDICAL DEVICE DRYER: (a) Model 135; (b) Model 136 Forced air dryer for medical devices; (a) Serial Numbers: 350423, 350424, 351506, 351507, 351512, 351513, 351514, 351516, 351602, 351604, 351605, 351606, 351609, 351611, 351613, 351614, 351615, 351616, 351617, 351618, 351619, 351620, 351621, 351622, 351623, 351624 (b) Serial numbers: 361505, 361511, 361515, 361601, 361603, 361607, 361608, 361612 | 34 units |
| Z-3033-2017 | ThermaSure(TM), a CENORIN(TM) product, SERIES 300 MEDICAL DEVICE DRYER: (a) Model 330; (b) Model 340 Forced air dryer for medical devices; (a) Serial Numbers: 331517, 331518, 331523, 331524, 331525, 331526, 331527, 331528, 331529, 331530, 331601, 331608, 331609, 331612, 331615, 331616, 331621, 331622, 331623, 331624, 331625, 331626, 331627 (b) Serial numbers: 341506, 341507, 341516, 341520, 341521, 341522, 341602, 341603, 341604, 341605, 341606, 341607, 341610, 341611, 341613, 341614, 341617, 341618, 341619, 341620 | 43 units |
| Z-3034-2017 | ThermaSure(TM), a CENORIN(TM) product, SERIES 1000 MEDICAL DEVICE DRYER: (a) Model 1009; (b) Model 1010 Forced air dryer for medical devices; (a) Serial Numbers: 191601, 191602, 191604, 191605, 19161, 191611, 191612, 191613, 191614, 191615, 191616 (b) Serial numbers: 101505, 101506, 101603, 101606, 101607, 101608, 101609 | 18 units |
What to do — step by step
Check Serial Number
Look for the serial number on your ThermaSure Series 300 dryer to see if it matches the list provided in the recall notice.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Worldwide Distribution - US (Nationwide) Internationally to Japan, Hong Kong, Brunei, and Israel” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 11 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-3033-2017 (June 7, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3033-2017 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.