Cenorin, LLC

Complete recall history across all FDA and CPSC categories — 6 total recalls

Cenorin, LLC appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (6)

FDA medical device enforcement actions by Cenorin, LLC

Date Product Reason Class
Apr 9, 2018 HLD Systems 600 Series Washer/Pasteurizer, UDI (01) 0085249007009 (11) 160929... There is a supplier quality issue with the terminal blocks which may cause th... Class II
Jun 7, 2017 ThermaSure(TM), a CENORIN(TM) product, SERIES 130 MEDICAL DEVICE DRYER: (a) M... Dryer unit not heating. Manufacturing issue causes the terminal block to ove... Class II
Jun 7, 2017 ThermaSure(TM), a CENORIN(TM) product, SERIES 1000 MEDICAL DEVICE DRYER: (a) ... Dryer unit not heating. Manufacturing issue causes the terminal block to ove... Class II
Jun 7, 2017 ThermaSure(TM), a CENORIN(TM) product, SERIES 300 MEDICAL DEVICE DRYER: (a) M... Dryer unit not heating. Manufacturing issue causes the terminal block to ove... Class II
Apr 24, 2014 HLD Systems Model 610 Washer/High Level Disinfector. Maximum weight of t... Cenorin LLC is voluntarily recalling HLD Systems Model 610 Washer/High Level ... Class II
Jan 24, 2013 HLD System, Model 610, Medical Device Cleaning and High Level Disinfection Wa... The temperature sensor/control system in the HLD Systems Model 610 may provid... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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