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AMD Medicom Inc.

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

AMD Medicom 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 (5)

FDA medical device enforcement actions by AMD Medicom Inc.

Date Product Reason Class
May 8, 2026 Ritmed Neurological Sponges, 0.75x0.75in, Sterile, REF: 85995C Neurological sponges used to moisten or absorb biological fluid during neurol... Class II
May 8, 2026 Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, Non-Sterile/55992C... Neurological sponges used to moisten or absorb biological fluid during neurol... Class II
Dec 21, 2023 HENRY SCHEIN¿ CRITERION¿ ANTI-FOG EARLOOP MASKS LEVEL 3 (BLUE) (item code 570... Level 3 masks were produced on alternate non-validated production equipment t... Class II
Dec 21, 2023 HENRY SCHEIN¿ CRITERION¿ EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448) Level 3 masks were produced on alternate non-validated production equipment t... Class II
Dec 21, 2023 PATTERSON¿ PROCEDURE EARLOOP MASKS- ANTI-FOG, ASTM LEVEL 3 (BLUE) (item code ... Level 3 masks were produced on alternate non-validated production equipment t... Class II
Oct 11, 2019 MEDICOM SAFEMASK PREMIER PLUS ASTM LEVEL 3 MASKS, Item Code 2042 Due to an error on the packaging line, some level 2 masks may have been packe... Class II
Oct 11, 2019 MEDICOM SAFEMASK PREMIER PLUS ASTM LEVEL 2 MASKS, Item Code 2040 Due to an error on the packaging line, some level 2 masks may have been packe... 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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