Manufacturer
179 recalls in our database name Medline Industries, Inc. as the manufacturing or recalling firm.
Of the 179 recalls from Medline Industries, Inc. we have scored against our rubric, 1 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 66 (37%) are Severe.
Which agencies issued them
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Medline Industries is recalling 190 units of pediatric elbow closed suction catheters because they were distributed before being sterilized.
Medline Industries is recalling Vitamin A&D Ointment packets that are incorrectly labeled as petroleum jelly. The outer boxes are correctly labeled.
Medline Industries is recalling 198 packs of 16 mm Distraction Pins because the sterile packaging seal may be compromised, risking loss of sterility.
Medline Industries is recalling 10 mm Distraction Pins because the sterile packaging seal may be compromised, potentially causing the device to lose sterility.
Medline Industries is recalling 14 mm Distraction Pins due to potential sterile packaging seal failures that could compromise device sterility.
Medline Industries is recalling 300 packs of 12 mm Distraction Pins because the sterile packaging seal may be compromised, potentially allowing the device to lose sterility.
Medline Industries is recalling 2,112 packs of sterile distraction pins because the packaging seal may be compromised, risking loss of sterility.
Medline Industries is recalling Unna-Z compression wraps due to contamination with common mold species. The recall affects units distributed in the US and several international countries.
Medline Industries is recalling 7,680 Rigid Suction Canisters (2000 CC and 3000 CC) because they may implode when subjected to excessive negative pressure.
Medline Industries is recalling 1-ounce medicine cups because the 10 mL increment is incorrectly printed as 5 mL, creating a risk of medication dosing errors.
Medline Industries is recalling 500 mg acetaminophen tablets mislabeled as 325 mg. Consumers should stop using the product and return it to the retailer.
Medline Industries is recalling 325 mg acetaminophen tablets that are actually 500 mg due to a labeling error.
Medline Industries is recalling Central Line kits due to a printing error that mislabels the intended patient age. The error could lead to use on the wrong patient population.
Medline is recalling 7,602 electrical surgical clippers because the charging base can overheat and smoke. The units were distributed in the U.S. and eight other countries.
Medline Industries is recalling 2,860 Esmark Elastic Bandages because they may not have been properly sterilized.
Medline Industries is recalling 1,610 mucus specimen traps because they may not be sterile, which could contaminate patient specimens.
Medline Industries is recalling 120 Cath Lab Custom Packs because the guidewire coating may flake off. The kits were distributed nationwide to specific states.
Medline Industries is recalling 112 surgical kits containing guidewires with a potential for coating to flake off.
Medline Industries is recalling 160 Heart Cath Custom Packs because a guidewire component may have a flaking coating.
Medline Industries is recalling 10 surgical kits containing guidewires with a potential coating defect. The kits were distributed to specific US states.
Medline Industries is recalling 120 surgical kits containing guidewires with a potential coating flaking defect.
Medline Industries is recalling 50 units of CATH ANGIOGRAPHY DRAPE PACKS because a guidewire inside the kits has a potential for its coating to flake off.
Medline Industries is recalling 304 surgical kits containing guidewires with a potential for coating to flake off.
Medline Industries is recalling 768 units of Angio Pack #2 surgical kits because a guidewire component has a potential for its coating to flake off.
Medline Industries is recalling five surgical kits containing a guidewire with a potential coating flake-off defect.
Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.
Medline Industries
American medical supply manufacturer and distributor
Source: Wikidata (Q6807236), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.