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Blood And Urine Collection Kit (Excludes Hiv Testing)

FDA product code OIB · Class 1 · Pathology

1,205
Registered devices
7
Adverse events
28
Recalls
0
510(k) clearances

Devices with this code

Aero-Med — AERO-MED, LLCAero-Med — AERO-MED, LLCKidney Health Test Kit 2 — Ditek Consulting, LLCAero-Med — AERO-MED, LLCCARDINAL HEALTH — AERO-MED, LLCAero-Med — AERO-MED, LLCMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.CARDINAL HEALTH — AERO-MED, LLCAero-Med — AERO-MED, LLCAero-Med — AERO-MED, LLCAero-Med — AERO-MED, LLCAero-Med — AERO-MED, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — AERO-MED, LLCAero-Med — AERO-MED, LLCAero-Med — AERO-MED, LLCAero-Med — AERO-MED, LLCCARDINAL HEALTH — AERO-MED, LLCAero-Med — AERO-MED, LLCAero-Med — AERO-MED, LLCMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.CARDINAL HEALTH — AERO-MED, LLCAero-Med — AERO-MED, LLC

Recent recalls

DateFirmReason
2026-07-20Medline Industries, LPDownstream recall - manufacturer recalled specific lots of BD ChloraPrep Clear - 1mL Applicators. Affected product may exhibit an open or incomplete seal on the
2026-06-12Medline Industries, LPThe kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in t
2026-06-12Medline Industries, LPThe kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in t
2026-03-16Medline Industries, LPMedline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal H
2026-03-09LSL Healthcare Inc.Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
2026-01-07Medline Industries, LPMedline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated ster
2026-01-07Medline Industries, LPMedline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated ster
2025-12-24Medline Industries, LPMedline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibi
2025-06-12MEDLINE INDUSTRIES, LP - NorthfieldAffected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. T
2024-04-08MEDLINE INDUSTRIES, LP - NorthfieldMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have bee

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.