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Civco Medical Instruments Inc

Complete recall history across all FDA and CPSC categories — 9 total recalls

Civco Medical Instruments Inc 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 (9)

FDA medical device enforcement actions by Civco Medical Instruments Inc

Date Product Reason Class
Feb 26, 2015 CIVCO Surgi-Tip Transducer Cover Sterile (15.2 x 244 cm) polyethylene telesco... Leaks were detected in the recalled lot which may compromise the sterility of... Class II
Aug 1, 2014 CollectEVAC, Sterile device with tubing and adaptor for use with ACMI and STO... A pinhole leak identified in the packaging of the recalled product potentiall... Class II
Oct 25, 2013 Civco Belly Board MRI, Reusable non-sterile glass fiber belly board with cush... Scales adhered to the product may be misaligned from the zero reference such ... Class II
Oct 25, 2013 Civco Belly Board, Reusable non-sterile carbon fiber belly board with cushion... Scales adhered to the product may be misaligned from the zero reference such ... Class II
May 7, 2012 CIVCO VirtuTRAX Instrument Navigator, Reusable non-sterile general purpose dr... The general purpose electromagnetic sensor was incorrectly calibrated causing... Class II
May 7, 2012 CIVCO General Purpose Sensor, Non-sterile reusable general purpose electromag... The general purpose electromagnetic sensor was incorrectly calibrated causing... Class II
May 7, 2012 CIVCO General Purpose Sensor, Non-sterile reusable general purpose electromag... The general purpose electromagnetic sensor was incorrectly calibrated causing... Class II
May 7, 2012 CIVCO General Purpose Sensor, Non-sterile reusable general purpose electromag... The general purpose electromagnetic sensor was incorrectly calibrated causing... Class II
May 7, 2012 CIVCO VirtuTRAX Instrument Navigator, Reusable non-sterile general purpose dr... The general purpose electromagnetic sensor was incorrectly calibrated causing... 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.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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