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Terminated

Advanced Instrument Model 2020 Multi-Sample Osmometer Intended to measure the osmotic pressure of body fluids.

FDA Recall Z-2068-2011 · Posted 2011-04-26

Recalling FirmAdvanced Instruments, Inc.
Recall StatusTerminated
Product CodeGKE
Date Initiated2011-01-19
Date Terminated2011-12-01
Product Quantity3 units

Reason for Recall

A poorly soldered power cord may pose a potential electrical shock hazard.

Firm Action

Advanced Instruments Product Service Department contacted each customer on 1/19/11 via an Urgent Product Recall Notice. The letter identified the reason for recall along with the affected products. The letter provided instructions to safely examine the date code of the AC Power Inlet assembly on the affected product. If customers were unable to perform the inspection or had questions concerning the instructions, they were to contact Advanced Instruments Product Service Manager at 781-471-2147 or via email [email protected]. The attached response forms were to be completed and returned as instructed.

Root Cause

Employee error

Distribution Pattern

Worldwide Distribution -- USA, including states of CA, GA IL, NJ, and MA and country of Belgium.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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