PlainRecalls
ModerateClass IITerminated

FDA Devices recall · Reported August 23, 2017

ThermaSure(TM), a CENORIN(TM) product, SERIES 130 MEDICAL DEVICE DRYER: (a) Model 135; (b) Model 136 Forced air dryer for medical devices

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

Recall #
Z-3032-2017
Affected scope
34 units
Initiated
June 7, 2017
Compiled from official public sources by the editorial team.
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Cenorin, LLC recalled ThermaSure(TM), a CENORIN(TM) product, SERIES 130 MEDICAL DEVICE DRYER: (a) Model 135; (b… - a moderate-severity action.

ThermaSure(TM), a CENORIN(TM) product, SERIES 130 MEDICAL DEVICE DRYER: (a) Model 135; (b… was recalled by Cenorin, LLC in August 23, 2017. Reason: Dryer unit not heating. Manufacturing issue causes the terminal block to overheat, char and/or burn.. Check the official notice for the remedy. Verify recall #Z-3032-2017 with the FDA Devices before acting.

The recall

Cenorin, LLC issued this moderate-severity FDA Devices recall-Dryer unit not heating. Manufacturing issue causes the terminal block to overheat, char and/or burn..

Moderate
severity level
34 units
affected scope
Class II
classification
August 23, 2017
reported

Sourced from official FDA Devices enforcement records. Verify recall #Z-3032-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Devices action (record #Z-3032-2017) was formally reported on August 23, 2017, with the manufacturer initiating the action on June 7, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. Cenorin, LLC is listed as the recalling firm, operating out of Kent, WA. Federal records list the affected scope as 34 units.

The documented reason for this recall is: Dryer unit not heating. Manufacturing issue causes the terminal block to overheat, char and/or burn. Distribution data in the federal record shows the product reached: Worldwide Distribution - US (Nationwide) Internationally to Japan, Hong Kong, Brunei, and Israel. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Medical Devices recalls over time

Where this recall sits in its category - 40,422 medical devices recalls on record

-1,00001,0002,0003,0004,0005,000 20052008201120142017202020232026 1,256
Severity2487872426High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Severity

Moderate

Affected scope

34 units

Related Recalls

6

0 from same agency

Product description

ThermaSure(TM), a CENORIN(TM) product, SERIES 130 MEDICAL DEVICE DRYER: (a) Model 135; (b) Model 136 Forced air dryer for medical devices

Reason for recall

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

Recall Profile

Structured summary of the FDA Devices recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number Z-3032-2017
Date reported August 23, 2017
Date initiated June 7, 2017
Recalling firm Cenorin, LLC
Firm location Kent, WA
Affected scope 34 units
Distribution Worldwide Distribution - US (Nationwide) Internationally to Japan, Hong Kong, Brunei, and Israel

Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

34 units units affected - limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units) -
Large-scale (100K – 1M units) -
Massive (≥1M units) -

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (Z-3032-2017) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Devices before acting, recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
ThermaSure(TM), a CENORIN(TM) product, SERIES 130 MEDICAL DEVICE DRYER: (a) Model 135; (b) Model 136 Forced air dryer for medical devices. Recalled by Cenorin, LLC. Units affected: 34 units.
Why was this product recalled?
Dryer unit not heating. Manufacturing issue causes the terminal block to overheat, char and/or burn.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 23, 2017. Severity: Moderate. Recall number: Z-3032-2017.
Where was the recalled product distributed?
Distribution: Worldwide Distribution - US (Nationwide) Internationally to Japan, Hong Kong, Brunei, and Israel.
How do I check if my product is affected by a recall?
Check the product description and recall number (Z-3032-2017) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device?
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nearby Recalls in This Category

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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported August 23, 2017. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.