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Owens & Minor Distribution, Inc.

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

Owens & Minor Distribution, 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 Owens & Minor Distribution, Inc.

Date Product Reason Class
Jan 3, 2023 FLUIDSHIELD 3 Fog-Free Procedure Mask with SO SOFT Lining and SO SOFT Earloop... Face masks were placed into the incorrect dispenser boxes. The face masks com... Class III
Oct 31, 2022 Aero Blue Performance Surgical Gown, XL- Sterile surgical gown Code: 41734 Potential open seal pouches compromising sterility resulting in the use of a ... Class II
Oct 31, 2016 Medi Choice Arm Slings ASL 2103 Small 7.5 x 12.5 Inch 1/EA, 24 ENCA ASL 2... Owens & Minor is the initial importer and private label distributor of Medi C... Class II
Nov 17, 2015 MediChoice Cohesive Bandages, One (1) roll of cohesive bandage per bag, thirt... MediChoice sterile cohesive bandages imported and sold under a private brand ... Class II
Nov 17, 2015 MediChoice Cohesive Bandages, One (1) roll of cohesive bandage per bag, thirt... MediChoice sterile cohesive bandages imported and sold under a private brand ... Class II
Nov 17, 2015 MediChoice Cohesive Bandages, One (1) roll of cohesive bandage per bag, thirt... MediChoice sterile cohesive bandages imported and sold under a private brand ... Class II
Jun 25, 2014 MediChoice Dual-Release Folding Walker with 5" wheel Product wheels may be too loose, too tight, or fall off. Class II
Mar 26, 2013 MediChoice¿ Rayon Tipped OB/GYN Applicator, 8 inch, Plastic Shaft, Non-Steril... Owens & Minor Distribution, Inc. is conducting a market withdrawal of MediCho... 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.

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