FDA recall record

Cenorin ThermaSure(TM), a CENORIN(TM) product, SERIES 300 MEDICAL DEVICE DRYER: (a) Model recall — FDA Z-3033-2017

Dryer unit not heating. Manufacturing issue causes the terminal block to overheat, char and/or burn.

Class IIclassification
Z-3033-2017official record ID
Aug 23, 2017report date

Recall record at a glance

Official recordZ-3033-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCenorin, LLC
Report dateAug 23, 2017
Recall initiation dateJun 7, 2017
Quantity43 units
LocationKent, WA, United States

Official product description

ThermaSure(TM), a CENORIN(TM) product, SERIES 300 MEDICAL DEVICE DRYER: (a) Model 330; (b) Model 340 Forced air dryer for medical devices

Why the product was recalled

Dryer unit not heating. Manufacturing issue causes the terminal block to overheat, char and/or burn.

Distribution information

Worldwide Distribution - US (Nationwide) Internationally to Japan, Hong Kong, Brunei, and Israel

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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