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Acumedia Manufacturers, Inc.

Complete recall history across all FDA and CPSC categories — 8 total recalls

Acumedia Manufacturers, 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 (8)

FDA medical device enforcement actions by Acumedia Manufacturers, Inc.

Date Product Reason Class
Aug 2, 2018 Campylobacter Blood Free Selective Medium, PN 7527A Used with cefoperazon... The product is labeled with an incorrect expiration date. Class III
Aug 2, 2018 Palcam Agar Base, Acumedia, PN 7669, Product Usage - Dehydrated culture media... Expiration date on the label is incorrect. Correct expiration date was Novemb... Class III
Sep 25, 2016 Urea Base Agar, Acumedia PN 7226 Urea Agar Base is used with agar for the di... Storage temperature listed on the label was incorrect. Label stated 2-30¿C. ... Class III
Aug 8, 2016 Sabouraud Dextrose Agar w /Lecithin and Tween 20 Acumedia PN 91081 Produc... Storage temperature listed on the label was incorrect. Label stated 2-30¿C. ... Class III
Apr 22, 2016 Tryptic Soy Agar, Acumedia PN 7100 500g, 2Kg, 10Kg, and 50Kg sizes light precipitate may form in prepared plates of Acumedia Tryptic Soy Agar (... Class II
Mar 23, 2016 Nutrient Gelatin, Acumedia Part Number 7471 A Product Usage: Nutrient Gel... Incorrect expiration date was listed on the label. Correct expiration date wa... Class III
Nov 30, 2015 Palcam Supplement Acumedia PN 7987 Product Usage: PALCAM Supplement is us... Contamination of product with possible Bacillus spp Class II
Sep 11, 2015 Beef Extract Powder, Acumedia PN 7228 Product Usage: Beef Extract Powder ... Incorrect expiration date on label. Correct expiration date was March 25, 20... Class III

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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