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MOOG Medical Devices Group

Complete recall history across all FDA and CPSC categories — 5 total recalls

MOOG Medical Devices Group 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 (5)

FDA medical device enforcement actions by MOOG Medical Devices Group

Date Product Reason Class
Dec 23, 2015 Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusi... Moog is recalling Curlin 4000, 6000, and PainSmart Infusion Pumps manufacture... Class II
Nov 20, 2015 Catalog No. INF0020-A  EnteraLite Infinity Enteral Pump Delivery Set with EN... Potential for leaking between the purple ENFit connector and the white transi... Class II
Nov 8, 2012 EnteraLite Infinity Enteral Feeding Pump identified with the following list n... MOOG Medical Devices Group is conducting a voluntary for a limited set of ser... Class II
Oct 12, 2012 Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum... The firm is adding an addendum to the operator's manual for Infinity Enterali... Class II
Sep 26, 2012 ***This recall is being conducted due to an incomplete recall for RES 57829**... This recall is the same issue for the FDA processed recall initiated by Moog ... 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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