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Quest Medical, Inc.

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

Quest Medical, 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 Quest Medical, Inc.

Date Product Reason Class
Jul 14, 2023 Q2 Multiport Extension set, REF: 9520, Rx Only Sterile, single use non-pyrog... For administration of intravenous fluids to a patient s vascular system utili... Class II
Dec 23, 2022 Precision Delivery Set with Filter, REF: PD06F; and Precision Delivery Set wi... Delivery Sets may have tubing that could become detached that could result in... Class II
Dec 17, 2019 Ref 801168, MPS Top Cover Replacement Kit, 1 UNITS, UDI: (01)2 0634624 81168... Additive and Arrest Agent Labels on the MPS Top Cover Replacement Kit, a repl... Class II
Oct 28, 2015 Model 5001102 MPS Delivery Set w/ arrest agent and additive cassettes, heat e... The products have been found to intermittently exhibit a seal failure during ... Class II
Feb 26, 2015 LIS27T - Lacrimal Intubation Set RX Only Sterile Used in various ophthal... Expiration date incorrectly printed in Manufacturing Date field on both pouch... 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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